3-aminocarbonyl/3-aminothiocarbonyl-substituted 2-benzoyl-cyclohexan-1,3-diones with herbicidal effect

ABSTRACT

The invention relates to 2-benzoylcyclohexane-1,3-diones of the formula I                    
     where 
     R 1 , R 2  are hydrogen, nitro, halogen, cyano, thiocyanato, alkyl, haloalkyl, alkoxyalkyl, alkenyl, alkynyl, —OR 5 , —OCOR 6 , —OSO 2 R 6 , —SH, —S(O) n R 7 , —SO 2 OR 5 , —SO 2 NR 5 R 8 , —NR 8 SO 2 R 6  or —NR 8 COR 6 ; 
     R 3  is hydrogen, alkyl, haloalkyl, alkenyl or alkynyl; 
     R 4  is hydrogen, unsubstituted or substituted alkyl, cycloalkyl, alkenyl, cycloalkenyl, alkynyl, —COR 9 , —CO 2 R 9 , —COSR 9  or —CONR 8 R 9 ; 
     X is oxygen or sulfur; 
     Z is oxygen or NR 8 ; 
     m is 0 or 1; 
     n is 0, 1 or 2; 
     R 5  is hydrogen, alkyl, haloalkyl, alkoxyalkyl, alkenyl or alkynyl; 
     R 6  is alkyl or haloalkyl; 
     R 7  is alkyl, haloalkyl, alkoxyalkyl, alkenyl or alkynyl; 
     R 8  is hydrogen or alkyl; 
     R 9  is alkyl, alkenyl, alkynyl, phenyl or benzyl; 
     R 10  is alkyl, haloalkyl, alkenyl or alkynyl; 
     Q is an unsubstituted or substituted cyclohexane-1,3-dione ring which is linked in the 2-position; 
     where m is 1 if R 3  is hydrogen; 
     and the agriculturally useful salts thereof; 
     processes and intermediates for the preparation of the compounds of the formula I; compositions comprising them; and the use of these derivatives or compositions comprising them for controlling undesired plants.

This application is a 371 of PCT/EP97/07211, filed Dec. 19, 1997.

The present invention relates to 2-benzoylcyclohexane-1,3-diones of the formula I

where the variables have the following meanings:

R¹, R² are hydrogen, nitro, halogen, cyano, thiocyanato, C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₁-C₆-alkoxy-C₁-C₆-alkyl, C₂-C₆-alkenyl, C₂-C₆-alkynyl, —OR⁵, —OCOR⁶, —OSO₂R⁶, —SH, —S(O)_(n)R⁷, —SO₂OR⁵, —SO₂NR⁵R⁸, —NR⁸SO₂R⁶ or —NR⁸COR⁶;

R³ is hydrogen, C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₃-C₆-alkenyl or C₃-C₆-alkynyl;

R⁴ is hydrogen, C₁-C₆-alkyl, C₃-C₆-cycloalkyl, C₃-C₆-alkenyl, C₄-C₆-cycloalkenyl, C₃-C₆-alkynyl, —COR⁹, —CO₂R⁹, —COSR⁹ or —CONR⁸R⁹, it being possible for the abovementioned alkyl, cycloalkyl, alkenyl, cycloalkenyl and alkynyl radicals and for R⁹ of the radicals —COR⁹, —CO₂R⁹, —COSR⁹ and —CONR⁸R⁹ to be partially or fully halogenated and/or to have attached to them one to three of the following groups:

 hydroxyl, mercapto, amino, cyano, R¹⁰, —OR¹⁰, —SR¹⁰, —NR⁸R¹⁰, ═NOR¹⁰, —OCOR¹⁰, —SCOR¹⁰, —NR⁸COR¹⁰, —CO₂R¹⁰, —COSR¹⁰, —CONR⁸R¹⁰, C₁-C₄-alkyliminooxy, C₁-C₄-alkoxyamino, C₁-C₄-alkylcarbonyl, C₁-C₄-alkoxy-C₂-C₆-alkoxycarbonyl, C₁-C₄-alkylsulfonyl, heterocyclyl, heterocyclyloxy, phenyl, phenyl-C₁-C₄-alkyl, hetaryl, phenoxy, phenyl-C₁-C₄-alkoxy and hetaryloxy, it being possible for the eight last-mentioned radicals, in turn, to be substituted;

X is oxygen or sulfur;

Z is oxygen or NR⁸;

m is 0 or 1;

n is 0, 1 or 2;

R⁵ is hydrogen, C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₁-C₆-alkoxy-C₂-C₆-alkyl, C₃-C₆-alkenyl or C₃-C₆-alkynyl;

R⁶ is C₁-C₆-alkyl or C₁-C₆-haloalkyl;

R⁷ is C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₁-C₆-alkoxy-C₂-C₆-alkyl, C₃-C₆-alkenyl or C₃-C₆-alkynyl;

R⁸ is hydrogen or C₁-C₆-alkyl;

R⁹ is C₁-C₆-alkyl, C₃-C₆-alkenyl, C₃-C₆-alkynyl, phenyl or benzyl;

R¹⁰ is C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₃-C₆-alkenyl or C₃-C₆-alkynyl;

Q is an unsubstituted or substituted cyclohexane-1,3-dione ring which is linked in the 2-position;

where m is 1 if R³ is hydrogen;

and to the agriculturally useful salts thereof.

Moreover, the invention relates to processes and to intermediates for the preparation of compounds of the formula I, to compositions comprising them, and to the use of the compounds of the formula I and of compositions comprising them for controlling harmful plants.

2-Benzoylcyclohexane-1,3-diones have been disclosed in the literature, for example in EP-A 278 742, EP-A 298 680, EP-A 320 864 and WO 96/14285.

However, the herbicidal properties of the prior-art compounds and their tolerance by crop plants are only moderately satisfactory.

It is an object of the present invention to provide novel, in particular herbicidally active, compounds which have improved properties.

We have found that this object is achieved by the 2-benzoylcyclohexane-1,3-diones of the formula I and their herbicidal activity.

Furthermore, there have been found herbicidal compositions which comprise the compounds I and which have a very good herbicidal activity. Moreover, there have been found processes for the preparation of these compositions and methods of controlling undesired vegetation using the compounds I.

Depending on the substitution pattern, the compounds of the formula I can also contain one or more chiral centers, in which case they are present as enantiomer or diastereomer mixtures. The invention relates to the pure enantiomers or diastereomers and also to mixtures of these.

The compounds of the formula I can also exist in the form of their agriculturally useful salts, the type of salt generally being unimportant. In general, suitable salts are salts of those cations or the acid addition salts of those acids whose cations, or anions, respectively, do not adversely affect the herbicidal activity of the compounds I.

Suitable cations are, in particular, ions of the alkali metals, preferably lithium, sodium and potassium, of the alkaline earth metals, preferably calcium and magnesium, and of the transition metals, preferably manganese, copper, zinc and iron, and also ammonium, it being possible in this case, if desired, for one to four hydrogen atoms to be replaced by C₁-C₄-alkyl or hydroxy-C₁-C₄-alkyl and/or a phenyl or benzyl, preferably diisopropylammonium, tetramethylammonium, tetrabutylammonium, trimethylbenzylammonium, in addition phosphonium ions, sulfonium ions, preferably tri(C₁-C₄-alkyl)sulfonium, and sulfoxonium ions, preferably tri(C₁-C₄-alkyl)sulfoxonium.

Anions of useful acid addition salts are mainly chloride, bromide, fluoride, hydrogen sulfate, sulfate, dihydrogen phosphate, hydrogen phosphate, nitrate, hydrogen carbonate, carbonate, hexafluorosilicate, hexafluorophosphate, benzoate, and the anions of C₁-C₄-alkanoic acids, preferably formate, acetate, propionate and butyrate.

Compounds of the formula I according to the invention to be emphasised are those where the variable Q is a cyclohexane-1,3-dione ring of the formula II

where II also represents the tautomeric formulae II′, and II″,

which is linked in the 2-position and where

R¹¹, R¹², R¹⁴ and R¹⁶ are hydrogen or C₁-C₄-alkyl;

R¹³ is hydrogen, C₁-C₄-alkyl or C₃-C₄-cycloalkyl, it being possible for the two last-mentioned groups to have attached to them one to three of the following substituents:

 halogen, C₁-C₄-alkylthio or C₁-C₄-alkoxy;

 or

 is tetrahydropyran-2-yl, tetrahydropyran-3-yl, tetrahydropyran-4-yl, tetrahydrothiopyran-2-yl, tetrahydrothiopyran-3-yl, tetrahydrothiopyran-4-yl, 1,3-dioxolan-2-yl, 1,3-dioxan-2-yl, 1,4-dioxan-2-yl, 1,3-oxathiolan-2-yl, 1,3-oxathian-2-yl, 1,3-dithiolan-2-yl or 1,3-dithian-2-yl, it being possible for the 6 last-mentioned radicals to be substituted by one to three C₁-C₄-alkyl radicals;

R¹⁵ is hydrogen, C₁-C₄-alkyl or C₁-C₆-alkoxycarbonyl;

 or

R¹³ and R¹⁶ together form a π bond or a three to six-membered carbocycylic ring;

 or

 the CR¹³R¹⁴ unit can be replaced by C═O.

Compounds of the formula I according to the invention equally to be emphasized are those where

R⁴ is hydrogen, C₁-C₆-alkyl, C₃-C₆-cycloalkyl, C₃-C₆-alkenyl, C₄-C₆-cycloalkenyl, C₃-C₆-alkynyl, —COR⁹, —CO₂R⁹, —COSR⁹ or —CONR⁸R⁹, it being possible for the abovementioned alkyl, cycloalkyl, alkenyl, cycloalkenyl and alkynyl radicals and for R⁹ of the radicals —COR⁹, —CO₂R⁹, —COSR⁹ and —CONR⁸R⁹ to be partially or fully halogenated and/or to have attached to them one to three of the following groups:

 hydroxyl, mercapto, amino, cyano, R¹⁰, —OR¹⁰, —SR¹⁰, —NR⁸R¹⁰, ═NOR¹⁰, —OCOR¹⁰, —SCOR¹⁰, —NR⁸COR¹⁰, —CO₂R¹⁰, —COSR¹⁰, —CONR⁸R¹⁰, C₁-C₄-alkyliminooxy, C₁-C₄-alkoxyamino, C₁-C₄-alkylcarbonyl, C₁-C₄-alkoxy-C₂-C₆-alkoxycarbonyl, C₁-C₄-alkylsulfonyl, heterocyclyl, heterocyclyloxy, phenyl, phenyl-C₁-C₄-alkyl, hetaryl, phenoxy, phenyl-C₁-C₄-alkoxy and hetaryloxy, it being possible for the eight last-mentioned radicals, in turn, to be partially or fully halogenated and/or to have attached to them one to three radicals selected from the group which follows:

 nitro, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy, C₁-C₄-alkoxycarbonyl.

The organic moieties mentioned for the substituents R¹-R¹⁶ or as radicals on phenyl, hetaryl and heterocyclyl rings are collective terms for individual enumerations of the individual group members. All hydrocarbon chains, ie. all alkyl, haloalkyl, cycloalkyl, alkoxyalkyl, alkoxy, haloalkoxy, alkyliminooxy, alkoxyamino, alkylthio, alkylsulfonyl, alkylcarbonyl, alkoxycarbonyl, alkoxyalkoxycarbonyl, alkenyl, cycloalkenyl, alkynyl moieties can be straight-chain or branched. Unless otherwise specified, halogenated substituents preferably have attached to them one to five identical or different halogen atoms. Halogen is in each case fluorine, chlorine, bromine or iodine.

Other examples of meanings are:

C₂-C₄-alkyl: ethyl, propyl, 1-methylethyl, butyl, 1-methylpropyl, 2-methylpropyl and 1,1-dimethylethyl;

C₁-C₄-alkyl, and the alkyl moieties of C₁-C₄-alkylcarbonyl: C₂-C₄-alkyl as mentioned above, and also methyl;

C₂-C₆-alkyl, and the alkyl moieties of C₁-C₆-alkoxy-C₂-C₆-alkyl: C₂-C₄-alkyl as mentioned above, and also pentyl, 1-methylbutyl, 2-methylbutyl, 3-methylbutyl, 2,2-dimethylpropyl, 1-ethylpropyl, hexyl, 1,1-dimethylpropyl, 1,2-dimethylpropyl, 1-methylpentyl, 2-methylpentyl, 3-methylpentyl, 4-methylpentyl, 1,1-dimethylbutyl, 1,2-dimethylbutyl, 1,3-dimethylbutyl, 2,2-dimethylbutyl, 2,3-dimethylbutyl, 3,3-dimethylbutyl, 1-ethylbutyl, 2-ethylbutyl, 1,1,2-trimethylpropyl, 1-ethyl-1-methylpropyl and 1-ethyl-3-methylpropyl;

C₁-C₆-alkyl, and the alkyl moieties of C₁-C₆-alkoxy-C₁-C₆-alkyl: C₂-C₆-alkyl as mentioned above, and also methyl;

C₁-C₄-haloalkyl: a C₁-C₄-alkyl radical as mentioned above which is partially or fully substituted by fluorine, chlorine, bromine and/or iodine, eg. chloromethyl, dichloromethyl, trichloromethyl, fluoromethyl, difluoromethyl, trifluoromethyl, chlorofluoromethyl, dichlorofluoromethyl, chlorodifluoromethyl, 2-fluoroethyl, 2-chloroethyl, 2-bromoethyl, 2-iodoethyl, 2,2-difluoroethyl, 2,2,2-trifluoroethyl, 2-chloro-2-fluoroethyl, 2-chloro-2,2-difluoroethyl, 2,2-dichloro-2-fluoroethyl, 2,2,2-trichloroethyl, pentafluoroethyl, 2-fluoropropyl, 3-fluoropropyl, 2,2-difluoropropyl, 2,3-difluoropropyl, 2-chloropropyl, 3-chloropropyl, 2,3-dichloropropyl, 2-bromopropyl, 3-bromopropyl, 3,3,3-trifluoropropyl, 3,3,3-trichloropropyl, 2,2,3,3,3-pentafluoropropyl, heptafluoropropyl, 1-(fluoromethyl)-2-fluoroethyl, 1-(chloromethyl)-2-chloroethyl, 1-(bromomethyl)-2-bromoethyl, 4-fluorobutyl, 4-chlorobutyl, 4-bromobutyl and nonafluorobutyl;

C₁-C₆-haloalkyl: C₁-C₄-haloalkyl as mentioned above, and also 5-fluoropentyl, 5-chloropentyl, 5-bromopentyl, 5-iodopentyl, undecafluoropentyl, 6-fluorohexyl, 6-chlorohexyl, 6-bromohexyl, 6-iodohexyl and dodecafluorohexyl;

C₁-C₄-alkoxy and the alkoxy moieties of C₁-C₄-alkoxyamino, C₁-C₄-alkoxy-C₂-C₆-alkoxycarbonyl and C₁-C₄-alkoxycarbonyl: methoxy, ethoxy, propoxy, 1-methylethoxy, butoxy, 1-methylpropoxy, 2-methylpropoxy and 1,1-dimethylethoxy;

C₁-C₆-alkoxy, and the alkoxy moieties of C₁-C₆-alkoxy-C₁-C₆-alkyl, C₁-C₄-alkoxy-C₂-C₆-alkoxycarbonyl and C₁-C₆-alkoxycarbonyl: C₁-C₄-alkoxy as mentioned above, and also pentoxy, 1-methylbutoxy, 2-methylbutoxy, 3-methoxylbutoxy [sic], 1,1-dimethylpropoxy, 1,2-dimethylpropoxy, 2,2-dimethylpropoxy, 1-ethylpropoxy, hexoxy, 1-methylpentoxy, 2-methylpentoxy, 3-methylpentoxy, 4-methylpentoxy, 1,1-dimethylbutoxy, 1,2-dimethylbutoxy, 1,3-dimethylbutoxy, 2,2-dimethylbutoxy, 2,3-dimethylbutoxy, 3,3-dimethylbutoxy, 1-ethylbutoxy, 2-ethylbutoxy, 1,1,2-trimethylpropoxy, 1,2,2-trimethylpropoxy, 1-ethyl-1-methylpropoxy and 1-ethyl-2-methylpropoxy;

C₁-C₄-haloalkoxy: a C₁-C₄-alkoxy radical as mentioned above which is partially or fully substituted by fluorine, chlorine, bromine and/or iodine, eg. fluoromethoxy, difluoromethoxy, trifluoromethoxy, chlorodifluoromethoxy, bromodifluoromethoxy, 2-fluoroethoxy, 2-chloroethoxy, 2-bromoethoxy, 2-iodoethoxy, 2,2-difluoroethoxy, 2,2,2-trifluoroethoxy, 2-chloro-2-fluoroethoxy, 2-chloro-2,2-difluoroethoxy, 2,2-dichloro-2-fluoroethoxy, 2,2,2-trichloroethoxy, pentafluoroethoxy, 2-fluoropropoxy, 3-fluoropropoxy, 2-chloropropoxy, 3-chloropropoxy, 2-bromopropoxy, 3-bromopropoxy, 2,2-difluoropropoxy, 2,3-difluoropropoxy, 2,3-dichloropropoxy, 3,3,3-trifluoropropoxy, 3,3,3-trichloropropoxy, 2,2,3,3,3-pentafluoropropoxy, heptafluoropropoxy, 1-(fluoromethyl)-2-fluoroethoxy, 1-(chloromethyl)-2-chloroethoxy, 1-(bromomethyl)-2-bromoethoxy, 4-fluorobutoxy, 4-chlorobutoxy, 4-bromobutoxy and nonafluorobutoxy;

C₁-C₄-alkylthio: methylthio, ethylthio, propylthio, 1-methylethylthio, butylthio, 1-methylpropylthio, 2-methylpropylthio and 1,1-dimethylethylthio;

C₁-C₄-alkylsulfonyl (C₁-C₄-alkyl-S(═O)₂-): methylsulfonyl, ethylsulfonyl, propylsulfonyl, 1-methylethylsulfonyl, butylsulfonyl, 1-methylpropylsulfonyl, 2-methylpropylsulfonyl and 1,1-dimethylethylsulfonyl;

C₁-C₄-alkyliminooxy: methyliminooxy, ethyliminooxy, 1-propyliminooxy, 2-propyliminooxy, 1-butyliminooxy and 2-butyliminooxy;

C₃-C₆-alkenyl: prop-1-en-1-yl, prop-2-en-1-yl, 1-methylethenyl, buten-1-yl, buten-2-yl, buten-3-yl, 1-methylprop-1-en-1-yl, 2-methylprop-1-en-1-yl, 1-methylprop-2-en-1-yl, 2-methylprop-2-en-1-yl, penten-1-yl, penten-2-yl, penten-3-yl, penten-4-yl, 1-methylbut-1-en-1-yl, 2-methylbut-1-en-1-yl, 3-methylbut-1-en-1-yl, 1-methylbut-2-en-1-yl, 2-methylbut-2-en-1-yl, 3-methylbut-2-en-1-yl, 1-methylbut-3-en-1-yl, 2-methylbut-3-en-1-yl, 3-methylbut-3-en-1-yl, 1,1-dimethylprop-2-en-1-yl, 1,2-dimethylprop-1-en-1-yl, 1,2-dimethylprop-2-en-1-yl, 1-ethylprop-1-en-2-yl, 1-ethylprop-2-en-1-yl, hex-1-en-1-yl, hex-2-en-1-yl, hex-3-en-1-yl, hex-4-en-1-yl, hex-5-en-1-yl, 1-methylpent-1-en-1-yl, 2-methylpent-1-en-1-yl, 3-methylpent-1-en-1-yl, 4-methylpent-1-en-1-yl, 1-methylpent-2-en-1-yl, 2-methylpent-2-en-1-yl, 3-methylpent-2-en-1-yl, 4-methylpent-2-en-1-yl, 1-methylpent-3-en-1-yl, 2-methylpent-3-en-1-yl, 3-methylpent-3-en-1-yl, 4-methylpent-3-en-1-yl, 1-methylpent-4-en-1-yl, 2-methylpent-4-en-1-yl, 3-methylpent-4-en-1-yl, 4-methylpent-4-en-1-yl, 1,1-dimethylbut-2-en-1-yl, 1,1-dimethylbut-3-en-1-yl, 1,2-dimethylbut-1-en-1-yl, 1,2-dimethylbut-2-en-1-yl, 1,2-dimethylbut-3-en-1-yl, 1,3-dimethylbut-1-en-1-yl, 1,3-dimethylbut-2-en-1-yl, 1,3-dimethylbut-3-en-1-yl, 2,2-dimethylbut-3-en-1-yl, 2,3-dimethylbut-1-en-1-yl, 2,3-dimethylbut-2-en-1-yl, 2,3-dimethylbut-3-en-1-yl, 3,3-dimethylbut-1-en-1-yl, 3,3-dimethylbut-2-en-1-yl, 1-ethylbut-1-en-1-yl, 1-ethylbut-2-en-1-yl, 1-ethylbut-3-en-1-yl, 2-ethylbut-1-en-1-yl, 2-ethylbut-2-en-1-yl, 2-ethylbut-3-en-1-yl, 1,1,2-trimethylprop-2-en-1-yl, 1-ethyl-1-methylprop-2-en-1-yl, 1-ethyl-2-methylprop-1-en-1-yl and 1-ethyl-2-methylprop-2-en-1-yl;

C₂-C₆-alkenyl: C₃-C₆-alkenyl as mentioned above, and also ethenyl;

C₃-C₆-alkynyl: prop-1-yn-1-yl, prop-2-yn-1-yl, but-1-yn-1-yl, but-1-yn-3-yl, but-1-yn-4-yl, but-2-yn-1-yl, pent-1-yn-1-yl, pent-1-yn-3-yl, pent-1-yn-4-yl, pent-1-yn-5-yl, pent-2-yn-1-yl, pent-2-yn-4-yl, pent-2-yn-5-yl, 3-methylbut-1-yn-3-yl, 3-methylbut-1-yn-4-yl, hex-1-yn-1-yl, hex-1-yn-3-yl, hex-1-yn-4-yl, hex-1-yn-5-yl, hex-1-yn-6-yl, hex-2-yn-1-yl, hex-2-yn-4-yl, hex-2-yn-5-yl, hex-2-yn-6-yl, hex-3-yn-1-yl, hex-3-yn-2-yl, 3-methylpent-1-yn-1-yl, 3-methylpent-1-yn-3-yl, 3-methylpent-1-yn-4-yl, 3-methylpent-1-yn-5-yl, 4-methylpent-1-yn-1-yl, 4-methylpent-2-yn-4-yl and 4-methylpent-2-yn-5-yl;

C₂-C₆-alkynyl: C₃-C₆-alkynyl as mentioned above, and also ethynyl;

C₃-C₄-cycloalkyl: cyclopropyl and cyclobutyl;

C₃-C₆-cycloalkyl: C₃-C₄-cycloalkyl as mentioned above, and also cyclopentyl and cyclohexyl;

C₄-C₆-cycloalkenyl: cyclobuten-1-yl, cyclobuten-3-yl, cyclopenten-1-yl, cyclopenten-3-yl, cyclopenten-4-yl, cyclohexen-1-yl, cyclohexen-3-yl and cyclohexen-4-yl;

heterocyclyl, and the heterocyclyl radicals in heterocyclyloxy: three to seven-membered saturated or partially unsaturated mono- or polycyclic heterocycles which contain one to three hetero atoms selected from a group consisting of oxygen, nitrogen and sulfur, such as oxiranyl, 2-tetrahydrofuranyl, 3-tetrahydrofuranyl, 2-tetrahydrothienyl, 3-tetrahydrothienyl, 2-pyrrolidinyl, 3-pyrrolidinyl, 3-isoxazolidinyl, 4-isoxazolidinyl, 5-isoxazolidinyl, 3-isothiazolidinyl, 4-isothiazolidinyl, 5-isothiazolidinyl, 3-pyrazolidinyl, 4-pyrazolidinyl, 5-pyrazolidinyl, 2-oxazolidinyl, 4-oxazolidinyl, 5-oxazolidinyl, 2-thiazolidinyl, 4-thiazolidinyl, 5-thiazolidinyl, 2-imidazolidinyl, 4-imidazolidinyl, 1,2,4-oxadiazolidin-3-yl, 1,2,4-oxadiazolidin-5-yl, 1,2,4-thiadiazolidin-3-yl, 1,2,4-thiadiazolidin-5-yl, 1,2,4-triazolidin-3-yl, 1,3,4-oxadiazolidin-2-yl, 1,3,4-thiadiazolidin-2-yl, 1,3,4-triazolidin-2-yl, 2,3-dihydrofuran-2-yl, 2,3-dihydrofuran-3-yl, 2,3-dihydrofuran-4-yl, 2,3-dihydrofuran-5-yl, 2,5-dihydrofuran-2-yl, 2,5-dihydrofuran-3-yl, 2,3-dihydrothien-2-yl, 2,3-dihydrothien-3-yl, 2,3-dihydrothien-4-yl, 2,3-dihydrothien-5-yl, 2,5-dihydrothien-2-yl, 2,5-dihydrothien-3-yl, 2,3-dihydropyrrol-2-yl, 2,3-dihydropyrrol-3-yl, 2,3-dihydropyrrol-4-yl, 2,3-dihydropyrrol-5-yl, 2,5-dihydropyrrol-2-yl, 2,5-dihydropyrrol-3-yl, 2,3-dihydroisoxazol-3-yl, 2,3-dihydroisoxazol-4-yl, 2,3-dihydroisoxazol-5-yl, 4,5-dihydroisoxazol-3-yl, 4,5-dihydroisoxazol-4-yl, 4,5-dihydroisoxazol-5-yl, 2,5-dihydroisoxazol-3-yl, 2,5-dihydroisoxazol-4-yl, 2,5-dihydroxazol-5-yl, 2,3-dihydroisothiazol-3-yl, 2,3-dihydroisothiazol-4-yl, 2,3-dihydroisothiazol-5-yl, 4,5-dihydroisothiazol-3-yl, 4,5-dihydroisothiazol-4-yl, 4,5-dihydroisothiazol-5-yl, 2,5-dihydroisothiazol-3-yl, 2,5-dihydroisothiazol-4-yl, 2,5-dihydroisothiazol-5-yl, 2,3-dihydropyrazol-3-yl, 2,3-dihydropyrazol-4-yl, 2,3-dihydropyrazol-5-yl, 4,5-dihydropyrazol-3-yl, 4,5-dihydropyrazol-4-yl, 4,5-dihydropyrazol-5-yl, 2,5-dihydropyrazol-3-yl, 2,5-dihydropyrazol-4-yl, 2,5-dihydropyrazol-5-yl, 2,3-dihydrooxazol-2-yl, 2,3-dihydrooxazol-4-yl, 2,3-dihydrooxazol-5-yl, 4,5-dihydrooxazol-2-yl, 4,5-dihydrooxazol-4-yl, 4,5-dihydrooxazol-5-yl, 2,5-dihydrooxazol-2-yl, 2,5-dihydrooxazol-4-yl, 2,5-dihydrooxazol-5-yl, 2,3-dihydrothiazol-2-yl, 2,3-dihydrothiazol-4-yl, 2,3-dihydrothiazol-5-yl, 4,5-dihydrothiazol-2-yl, 4,5-dihydrothiazol-4-yl, 4,5-dihydrothiazol-5-yl, 2,5-dihydrothiazol-2-yl, 2,5-dihydrothiazol-4-yl, 2,5-dihydrothiazol-5-yl, 2,3-dihydroimidazol-2-yl, 2,3-dihydroimidazol-4-yl, 2,3-dihydroimidazol-5-yl, 4,5-dihydroimidazol-2-yl, 4,5-dihydroimidazol-4-yl, 4,5-dihydroimidazol-5-yl, 2,5-dihydroimidazol-2-yl, 2,5-dihydroimidazol-4-yl, 2,5-dihydroimidazol-5-yl, 2-morpholinyl, 3-morpholinyl, 2-piperidinyl, 3-piperidinyl, 4-piperidinyl, 3-tetrahydropyridazinyl, 4-tetrahydropyridazinyl, 2-tetrahydropyrimidinyl, 4-tetrahydropyrimidinyl, 5-tetrahydropyrimidinyl, 2-tetrahydropyrazinyl, 1,3,5-tetrahydrotriazin-2-yl, 1,2,4-tetrahydrotriazin-3-yl, 1,3-dihydrooxazin-2-yl, 1,3-dithian-2-yl, 2-tetrahydropyranyl, 3-tetrahydropyranyl, 4-tetrahydropyranyl, 2-tetrahydrothiopyranyl, 3-tetrahydrothiopyranyl, 4-tetrahydrothiopyranyl, 1,3-dioxolan-2-yl, 3,4,5,6-tetrahydropyridin-2-yl, 4H-1,3-thiazin-2-yl, 4H-3,1-benzothiazin-2-yl, 1,1-dioxo-2,3,4,5-tetrahydrothien-2-yl, 2H-1,4-benzothiazin-3-yl, 2H-1,4-benzoxazin-3-yl, 1,3-dihydrooxazin-2-yl,

hetaryl, and the hetaryl radicals in hetaryloxy: aromatic mono- or polycyclic radicals which, besides carbon ring members, additionally can contain one to four nitrogen atoms or one to three nitrogen atoms and an oxygen or a sulfur atom or an oxygen or a sulfur atom, eg. 2-furyl, 3-furyl, 2-thienyl, 3-thienyl, 2-pyrrolyl, 3-pyrrolyl, 3-isoxazolyl, 4-isoxazolyl, 5-isoxazolyl, 3-isothiazolyl, 4-isothiazolyl, 5-isothiazolyl, 3-pyrazolyl, 4-pyrazolyl, 5-pyrazolyl, 2-oxazolyl, 4-oxazolyl, 5-oxazolyl, 2-thiazolyl, 4-thiazolyl, 5-thiazolyl, 2-imidazolyl, 4-imidazolyl, 1,2,4-oxadiazol-3-yl, 1,2,4-oxadiazol-5-yl, 1,2,4-thiadiazol-3-yl, 1,2,4-thiadiazol-5-yl, 1,2,4-triazol-3-yl, 1,3,4-oxadiazol-2-yl, 1,3,4-thiadiazol-2-yl, 1,3,4-triazol-2-yl, 2-pyridinyl, 3-pyridinyl, 4-pyridinyl, 3-pyridazinyl, 4-pyridazinyl, 2-pyrimidinyl, 4-pyrimidinyl, 5-pyrimidinyl, 2-pyrazinyl, 1,3,5-triazin-2-yl, 1,2,4-triazin-3-yl, 1,2,4,5-tetrazin-3-yl, and the corresponding benzo-fused derivatives.

All phenyl and hetaryl rings are preferably unsubstituted or have attached to them one to three halogen atoms and/or one or two radicals selected from the group which follows: nitro, cyano, methyl, trifluoromethyl, methoxy, trifluoromethoxy and methoxycarbonyl.

With a view to the use of the compounds of the formula I according to the invention as herbicides, the variables preferably have the following meanings, in each case alone or in combination:

R¹ is nitro, halogen, cyano, thiocyanato, C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₁-C₆-alkoxy-C₁-C₆-alkyl, C₂-C₆-alkenyl, C₂-C₆-alkynyl, —OR⁵ or —S(O)_(n)R⁷;

 especially preferably nitro, halogen, eg. fluorine, chlorine or bromine, C₁-C₆-haloalkyl, eg. trifluoromethyl, —OR⁵ or —SO₂R⁷;

R² is hydrogen, nitro, halogen, cyano, thiocyanato, C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₁-C₆-alkoxy-C₁-C₆-alkyl, C₂-C₆-alkenyl, C₂-C₆-alkynyl, —OR⁵ or —S(O)_(n)R⁷;

 especially preferably hydrogen, nitro, halogen, eg. fluorine, chlorine or bromine, C₁-C₆-alkyl, eg. methyl or ethyl, C₁-C₆-haloalkyl, eg. trifluoromethyl, —OR⁵ or —SO₂R⁷;

R³ is hydrogen, C₁-C₆-alkyl, eg. methyl, ethyl, propyl or butyl, or C₁-C₆-haloalkyl, eg. difluoromethyl or trifluoromethyl;

R⁴ is hydrogen, C₁-C₆-alkyl, C₃-C₆-cycloalkyl, C₃-C₆-alkenyl or C₃-C₆-alkynyl, it being possible for the 4 last-mentioned substituents to be partially or fully halogenated and/or to have attached to them one to three of the following groups: hydroxyl, mercapto, amino, cyano, —OR¹⁰, ═NOR¹⁰, —OCOR¹⁰, —CO₂R¹⁰, —COSR¹⁰, —CONR⁸R¹⁰, C₁-C₄-alkyliminooxy, C₁-C₄-alkylcarbonyl, C₁-C₄-alkoxy-C₂-C₆-alkoxycarbonyl, heterocyclyl, heterocyclyloxy, phenyl, phenyl-C₁-C₄-alkyl, hetaryl, phenoxy, phenyl-C₁-C₄-alkoxy or hetaryloxy, it being possible for the eight last-mentioned radicals, in turn, to be partially or fully halogenated and/or to have attached to them one to three radicals selected from the group which follows:

 nitro, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy, C₁-C₄-alkoxycarbonyl;

 X is oxygen or sulfur;

 especially preferably oxygen;

Z is oxygen, NH or NCH₃;

m is 0 or 1

n is 0 or 2

R⁵ is hydrogen, C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₁-C₆-alkoxy-C₂-C₆-alkyl, C₃-C₆-alkenyl or C₃-C₆-alkynyl;

 especially preferably methyl, ethyl, trifluoromethyl, difluoromethyl, methoxyethyl, allyl or propargyl;

R⁷ is C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₁-C₆-alkoxy-C₂-C₆-alkyl, C₃-C₆-alkenyl or C₃-C₆-alkynyl;

 especially preferably methyl, ethyl, trifluoromethyl, difluoromethyl, methoxyethyl, allyl or propargyl;

R⁸ is hydrogen or C₁-C₆-alkyl;

R¹⁰ is C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₃-C₆-alkenyl or C₃-C₆-alkynyl;

R¹¹, R¹², R¹⁴, R¹⁶ are hydrogen or C₁-C₄-alkyl;

 especially preferably hydrogen, methyl or ethyl;

R¹³ is hydrogen, C₁-C₄-alkyl, C₃-C₄-cycloalkyl, it being possible for the two last-mentioned groups to be unsubstituted or to have attached to them one to three of the following substituents: halogen, C₁-C₄-alkoxy or C₁-C₄-alkylthio;

 tetrahydropyran-2-yl, tetrahydropyran-3-yl, tetrahydropyran-4-yl, tetrahydrothiopyran-2-yl, tetrahydrothiopyran-3-yl, tetrahydrothiopyran-4-yl, 1,3-dioxolan-2-yl, 1,3-dioxan-2-yl, 1,4-dioxan-2-yl, 1,3-oxathiolan-2-yl, 1,3-oxathian-2-yl, 1,3-dithian-2-yl or 1,3-dithiolan-2-yl, it being possible for the six last-mentioned groups to have attached to them in each case one to three C₁-C₄-alkyl radicals;

 especially preferably hydrogen, methyl, ethyl, cyclopropyl, di(methoxy)methyl, di(ethoxy)methyl, 2-ethylthiopropyl, tetrahydropyran-2-yl, tetrahydropyran-3-yl, tetrahydropyran-4-yl, tetrahydrothiopyran-2-yl, tetrahydrothiopyran-3-yl, tetrahydrothiopyran-4-yl, 1,3-dioxolan-2-yl, 1,3-dioxan-2-yl, 1,4-dioxan-2-yl, 5,5-dimethyl-1-3-dioxan-2-yl, 1,3-oxathiolan-2-yl, 1,3-oxathian-2-yl, 1,3-dithiolan-2-yl, 5,5-dimethyl-1,3-dithian-2-yl or 1-methylthiocyclopropyl;

R¹⁵ is hydrogen, C₁-C₄-alkyl or C₁-C₄-alkoxycarbonyl;

 especially preferably hydrogen, methyl or methoxycarbonyl.

Equally, it may be advantageous for R¹³ and R¹⁶ to form a π bond so that a double bond system results.

Also, the CR¹³R¹⁴ unit can be replaced advantageously by C═O.

Especially preferred compounds of the formula I are where m=1. Also especially preferred are compounds where m=0 and R³, R⁴ ≠ hydrogen.

Particularly preferred compounds of the formula I are those where m=1.

Extraordinarily preferred are compounds of the formula Ia ({circumflex over (=)} I where R¹ is bonded in the 4-position of the phenyl ring and R² in the 2-position of the phenyl ring).

Particularly extraordinarily preferred are the compounds of the formula Ia where the variables R¹ to R³, Q, X, Z and m have the meanings mentioned above and

R⁴ is hydrogen, C₁-C₆-alkyl, C₃-C₆-cycloalkyl, C₃-C₆-alkenyl or C₃-C₆-alkynyl, it being possible for the 4 last-mentioned substituents to be partially or fully halogenated and/or to have attached to them one to three of the following groups: hydroxyl, mercapto, amino, cyano, —OR¹⁰, ═NOR¹⁰, —OCOR¹⁰, —CO₂R¹⁰, —COSR¹⁰, —CONR⁸R¹⁰, C₁-C₄-alkyliminooxy, C₁-C₄-alkylcarbonyl, C₁-C₄-alkoxy-C₂-C₆-alkoxycarbonyl, heterocyclyl, heterocyclyloxy, phenyl, phenyl-C₁-C₄-alkyl, hetaryl, phenoxy, phenyl-C₁-C₄-alkoxy or hetaryloxy, it being possible for the eight last-mentioned radicals, in turn, to be partially or fully halogenated and/or to have attached to them one to three radicals selected from the group which follows:

 nitro, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy, C₁-C₄-alkoxycarbonyl.

Most particularly most extraordinarily preferred are the compounds Ia1 ({circumflex over (=)} I where R¹=C1, R¹¹, R¹², R¹³, R¹⁴, R¹⁵, R¹⁶=H, X=oxygen and m=1, where R¹ is bonded in the 4-position of the phenyl ring and R² in the 2-position of the phenyl ring), in particular the compounds of Table 1.

TABLE 1 No. R² R³ R⁴ Z Ia1.1 Cl H CH₃ O Ia1.2 Cl CH₃ CH₃ O Ia1.3 Cl CH₂CH₃ CH₃ O Ia1.4 Cl (CH₂)₂CH₃ CH₃ O Ia1.5 Cl (CH₂)₃CH₃ CH₃ O Ia1.6 Cl H C₂H₅ O Ia1.7 Cl CH₃ C₂H₅ O Ia1.8 Cl CH₂CH₃ C₂H₅ O Ia1.9 Cl (CH₂)₂CH₃ C₂H₅ O Ia1.10 Cl (CH₂)₃CH₃ C₂H₅ O Ia1.11 Cl H (CH₂)₂CH₃ O Ia1.12 Cl CH₃ (CH₂)₂CH₃ O Ia1.13 Cl CH₂CH₃ (CH₂)₂CH₃ O Ia1.14 Cl (CH₂)₂CH₃ (CH₂)₂CH₃ O Ia1.15 Cl (CH₂)₃CH₃ (CH₂)₂CH₃ O Ia1.16 Cl H CH(CH₃)₂ O Ia1.17 Cl CH₃ CH(CH₃)₂ O Ia1.18 Cl CH₂CH₃ CH(CH₃)₂ O Ia1.19 Cl (CH₂)₂CH₃ CH(CH₃)₂ O Ia1.20 Cl (CH₂)₃CH₃ CH(CH₃)₂ O Ia1.21 Cl H (CH₂)₃CH₃ O Ia1.22 Cl CH₃ (CH₂)₃CH₃ O Ia1.23 Cl CH₂CH₃ (CH₂)₃CH₃ O Ia1.24 Cl (CH₂)₂CH₃ (CH₂)₃CH₃ O Ia1.25 Cl (CH₂)₃CH₃ (CH₂)₃CH₃ O Ia1.26 Cl H CH₂CH(CH₃)₂ O Ia1.27 Cl CH₃ CH₂CH(CH₃)₂ O Ia1.28 Cl CH₂CH₃ CH₂CH(CH₃)₂ O Ia1.29 Cl (CH₂)₂CH₃ CH₂CH(CH₃)₂ O Ia1.30 Cl (CH₂)₃CH₃ CH₂CH(CH₃)₂ O Ia1.31 Cl H CH(CH₃)CH₂CH₃ O Ia1.32 Cl CH₃ CH(CH₃)CH₂CH₃ O Ia1.33 Cl CH₂CH₃ CH(CH₃)CH₂CH₃ O Ia1.34 Cl (CH₂)₂CH₃ CH(CH₃)CH₂CH₃ O Ia1.35 Cl (CH₂)₃CH₃ CH(CH₃)CH₂CH₃ O Ia1.36 Cl H (CH₂)₂—C₆H₅ O Ia1.37 Cl CH₃ (CH₂)₂—C₆H₅ O Ia1.38 Cl CH₂CH₃ (CH₂)₂—C₆H₅ O Ia1.39 Cl (CH₂)₂CH₃ (CH₂)₂—C₆H₅ O Ia1.40 Cl (CH₂)₃CH₃ (CH₂)₂—C₆H₅ O Ia1.41 Cl H CH₂CH(CH₃)—C₆H₅ O Ia1.42 Cl CH₃ CH₂CH(CH₃)—C₆H₅ O Ia1.43 Cl CH₂CH₃ CH₂CH(CH₃)—C₆H₅ O Ia1.44 Cl (CH₂)₂CH₃ CH₂CH(CH₃)—C₆H₅ O Ia1.45 Cl (CH₂)₃CH₃ CH₂CH(CH₃)—C₆H₅ O Ia1.46 Cl H CH(CH₃)CH₂—C₆H₅ O Ia1.47 Cl CH₃ CH(CH₃)CH₂—C₆H₅ O Ia1.48 Cl CH₂CH₃ CH(CH₃)CH₂—C₆H₅ O Ia1.49 Cl (CH₂)₂CH₃ CH(CH₃)CH₂—C₆H₅ O Ia1.50 Cl (CH₂)₃CH₃ CH(CH₃)CH₂—C₆H₅ O Ia1.51 Cl H CH(CH₃)CH(CH₃)—C₆H₅ O Ia1.52 Cl CH₃ CH(CH₃)CH(CH₃)—C₆H₅ O Ia1.53 Cl CH₂CH₃ CH(CH₃)CH(CH₃)—C₆H₅ O Ia1.54 Cl (CH₂)₂CH₃ CH(CH₃)CH(CH₃)—C₆H₅ O Ia1.55 Cl (CH₂)₃CH₃ CH(CH₃)CH(CH₃)—C₆H₅ O Ia1.56 Cl H (CH₂)₂-(4-Cl—C₆H₄) O Ia1.57 Cl CH₃ (CH₂)₂-(4-Cl—C₆H₄) O Ia1.58 Cl CH₂CH₃ (CH₂)₂-(4-Cl—C₆H₄) O Ia1.59 Cl (CH₂)₂CH₃ (CH₂)₂-(4-Cl—C₆H₄) O Ia1.60 Cl (CH₂)₃CH₃ (CH₂)₂-(4-Cl—C₆H₄) O Ia1.61 Cl H CH₂CH(CH₃)-(4-Cl—C₆H₄) O Ia1.62 Cl CH₃ CH₂CH(CH₃)-(4-Cl—C₆H₄) O Ia1.63 Cl CH₂CH₃ CH₂CH(CH₃)-(4-Cl—C₆H₄) O Ia1.64 Cl (CH₂)₂CH₃ CH₂CH(CH₃)-(4-Cl—C₆H₄) O Ia1.65 Cl (CH₂)₃CH₃ CH₂CH(CH₃)-(4-Cl—C₆H₄) O Ia1.66 Cl H CH(CH₃)CH₂-(4-Cl—C₆H₄) O Ia1.67 Cl CH₃ CH(CH₃)CH₂-(4-Cl—C₆H₄) O Ia1.68 Cl CH₂CH₃ CH(CH₃)CH₂-(4-Cl—C₆H₄) O Ia1.69 Cl (CH₂)₂CH₃ CH(CH₃)CH₂-(4-Cl—C₆H₄) O Ia1.70 Cl (CH₂)₃CH₃ CH(CH₃)CH₂-(4-Cl—C₆H₄) O Ia1.71 Cl H CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) O Ia1.72 Cl CH₃ CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) O Ia1.73 Cl CH₂CH₃ CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) O Ia1.74 Cl (CH₂)₂CH₃ CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) O Ia1.75 Cl (CH₂)₃CH₃ CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) O Ia1.76 Cl H (CH₂)₂-(2,4-Cl₂—C₆H₃₎ O Ia1.77 Cl CH₃ (CH₂)₂-(2,4-Cl₂—C₆H₃₎ O Ia1.78 Cl CH₂CH₃ (CH₂)₂-(2,4-Cl₂—C₆H₃) O Ia1.79 Cl (CH₂)₂CH₃ (CH₂)₂-(2,4-Cl₂—C₆H₃) O Ia1.80 Cl (CH₂)₃CH₃ (CH₂)₂-(2,4-Cl₂—C₆H₃) O Ia1.81 Cl H CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) O Ia1.82 Cl CH₃ CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) O Ia1.83 Cl CH₂CH₃ CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) O Ia1.84 Cl (CH₂)₂CH₃ CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) O Ia1.85 Cl (CH₂)₃CH₃ CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) O Ia1.86 Cl H CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) O Ia1.87 Cl CH₃ CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) O Ia1.88 Cl CH₂CH₃ CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) O Ia1.89 Cl (CH₂)₂CH₃ CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) O Ia1.90 Cl (CH₂)₃CH₃ CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) O Ia1.91 Cl H CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) O Ia1.92 Cl CH₃ CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) O Ia1.93 Cl CH₂CH₃ CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) O Ia1.94 Cl (CH₂)₂CH₃ CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) O Ia1.95 Cl (CH₂)₃CH₃ CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) O Ia1.96 Cl H (CH₂)₂—O—C₆H₅ O Ia1.97 Cl CH₃ (CH₂)₂—O—C₆H₅ O Ia1.98 Cl CH₂CH₃ (CH₂)₂—O—C₆H₅ O Ia1.99 Cl (CH₂)₂CH₃ (CH₂)₂—O—C₆H₅ O Ia1.100 Cl (CH₂)₃CH₃ (CH₂)₂—O—C₆H₅ O Ia1.101 Cl H CH₂CH(CH₃)—O—C₆H₅ O Ia1.102 Cl CH₃ CH₂CH(CH₃)—O—C₆H₅ O Ia1.103 Cl CH₂CH₃ CH₂CH(CH₃)—O—C_(6H) ₅ O Ia1.104 Cl (CH₂)₂CH₃ CH₂CH(CH₃)—O—C₆H₅ O Ia1.105 Cl (CH₂)₃CH₃ CH₂CH(CH₃)—O—C₆H₅ O Ia1.106 Cl H CH(CH₃)CH₂—O—C₆H₅ O Ia1.107 Cl CH₃ CH(CH₃)CH₂—O—C₆H₅ O Ia1.108 Cl CH₂CH₃ CH(CH₃)CH₂—O—C₆H₅ O Ia1.109 Cl (CH₂)₂CH₃ CH(CH₃)CH₂—O—C₆H₅ O Ia1.110 Cl (CH₂)₃CH₃ CH(CH₃)CH₂—O—C₆H₅ O Ia1.111 Cl H CH(CH₃)CH(CH₃)—O—C₆H₅ O Ia1.112 Cl CH₃ CH(CH₃)CH(CH₃)—O—C₆H₅ O Ia1.113 Cl CH₂CH₃ CH(CH₃)CH(CH₃)—O—C₆H₅ O Ia1.114 Cl (CH₂)₂CH₃ CH(CH₃)CH(CH₃)—O—C₆H₅ O Ia1.115 Cl (CH₂)₃CH₃ CH(CH₃)CH(CH₃)—O—C₆H₅ O Ia1.116 Cl H (CH₂)₂—O-(4-Cl—C₆H₄) O Ia1.117 Cl CH₃ (CH₂)₂—O-(4-Cl—C₆H₄) O Ia1.118 Cl CH₂CH₃ (CH₂)₂—O-(4-Cl—C₆H₄) O Ia1.119 Cl (CH₂)₂CH₃ (CH₂)2—O-(4-Cl—C₆H₄) O Ia1.120 Cl (CH₂)₃CH₃ (CH₂)2—O-(4-Cl—C₆H₄) O Ia1.121 Cl H CH₂CH(CH₃)—O-(4-Cl-C₆H₄) O Ia1.122 Cl CH₃ CH₂CH(CH₃)—O-(4-Cl-C₆H₄) O Ia1.123 Cl CH₂CH₃ CH₂CH(CH₃)—O-(4-Cl-C₆H₄) O Ia1.124 Cl (CH₂)₂CH₃ CH₂CH(CH₃)—O-(4-Cl-C₆H₄) O Ia1.125 Cl (CH₂)₃CH₃ CH₂CH(CH₃)—O-( 4-Cl—C₆H₄) O Ia1.126 Cl H CH(CH₃)CH₂—O-(4-Cl-C₆H₄) O Ia1.127 Cl CH₃ CH(CH₃)CH₂—O-(4-Cl-C₆H₄) O Ia1.128 Cl CH₂CH₃ CH(CH₃)CH₂—O-(4-Cl—C₆H₄) O Ia1.129 Cl (CH₂)₂CH₃ CH(CH₃)CH₂—O-(4-Cl—C₆H₄) O Ia1.130 Cl (CH₂)₃CH₃ CH(CH₃)CH₂—O-(4-Cl—C₆H₄) O Ia1.131 Cl H CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) O Ia1.132 Cl CH₃ CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) O Ia1.133 Cl CH₂CH₃ CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) O Ia1.134 Cl (CH₂)₂CH₃ CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) O Ia1.135 Cl (CH₂)₃CH₃ CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) O Ia1.136 Cl H (CH₂)₂—O-(2,4-Cl₂—C₆H₃) O Ia1.137 Cl CH₃ (CH₂)₂—O-(2,4-Cl₂—C₆H₃) O Ia1.138 Cl CH₂CH₃ (CH₂)₂—O-(2,4-Cl₂—C₆H₃) O Ia1.139 Cl (CH₂)₂CH₃ (CH₂)₂—O-(2,4-Cl₂—C₆H₃) O Ia1.140 Cl (CH₂)₃CH₃ (CH₂)₂—O-(2,4-Cl₂—C₆H₃) O Ia1.141 Cl H CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) O Ia1.142 Cl CH₃ CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) O Ia1.143 Cl CH₂CH₃ CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) O Ia1.144 Cl (CH₂)₂CH₃ CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) O Ia1.145 Cl (CH₂)₃CH₃ CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) O Ia1.146 Cl H CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) O Ia1.147 Cl CH₃ CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) O Ia1.148 Cl CH₂CH₃ CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) O Ia1.149 Cl (CH₂)₂CH₃ CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) O Ia1.150 Cl (CH₂)₃CH₃ CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) O Ia1.151 Cl H CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) O Ia1.152 Cl CH₃ CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) O Ia1.153 Cl CH₂CH₃ CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) O Ia1.154 Cl (CH₂)₂CH₃ CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) O Ia1.155 Cl (CH₂)₃CH₃ CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) O Ia1.156 Cl H CH₃ NH Ia1.157 Cl CH₃ CH₃ NH Ia1.158 Cl CH₂CH₃ CH₃ NH Ia1.159 Cl (CH₂)₂CH₃ CH₃ NH Ia1.160 Cl (CH₂)₃CH₃ CH₃ NH Ia1.161 Cl H C₂H₅ NH Ia1.162 Cl CH₃ C₂H₅ NH Ia1.163 Cl CH₂CH₃ C₂H₅ NH Ia1.164 Cl (CH₂)₂CH₃ C₂H₅ NH Ia1.165 Cl (CH₂)₃CH₃ C₂H₅ NH Ia1.166 Cl H (CH₂)₂CH₃ NH Ia1.167 Cl CH₃ (CH₂)₂CH₃ NH Ia1.168 Cl CH₂CH₃ (CH₂)₂CH₃ NH Ia1.169 Cl (CH₂)₂CH₃ (CH₂)₂CH₃ NH Ia1.170 Cl (CH₂)₃CH₃ (CH₂)₂CH₃ NH Ia1.171 Cl H CH(CH₃)₂ NH Ia1.172 Cl CH₃ CH(CH₃)₂ NH Ia1.173 Cl CH₂CH₃ CH(CH₃)₂ NH Ia1.174 Cl (CH₂)₂CH₃ CH(CH₃)₂ NH Ia1.175 Cl (CH₂)₃CH₃ CH(CH₃)₂ NH Ia1.176 Cl H (CH₂)₃CH₃ NH Ia1.177 Cl CH₃ (CH₂)₃CH₃ NH Ia1.178 Cl CH₂CH₃ (CH₂)₃CH₃ NH Ia1.179 Cl (CH₂)₂CH₃ (CH₂)₃CH₃ NH Ia1.180 Cl (CH₂)₃CH₃ (CH₂)₃CH₃ NH Ia1.181 Cl H CH₂CH(CH₃)₂ NH Ia1.182 Cl CH₃ CH₂CH(CH₃)₂ NH Ia1.183 Cl CH₂CH₃ CH₂CH(CH₃)₂ NH Ia1.184 Cl (CH₂)₂CH₃ CH₂CH(CH₃)₂ NH Ia1.185 Cl (CH₂)₃CH₃ CH₂CH(CH₃)₂ NH Ia1.186 Cl H CH(CH₃)CH₂CH₃ NH Ia1.187 Cl CH₃ CH(CH₃)CH₂CH₃ NH Ia1.188 Cl CH₂CH₃ CH(CH₃)CH₂CH₃ NH Ia1.189 Cl (CH₂)₂CH₃ CH(CH₃)CH₂CH₃ NH Ia1.190 Cl (CH₂)₃CH₃ CH(CH₃)CH₂CH₃ NH Ia1.191 Cl H (CH₂)₂—C₆H₅ NH Ia1.192 Cl CH₃ (CH₂)₂—C₆H₅ NH Ia1.193 Cl CH₂CH₃ (CH₂)₂—C₆H₅ NH Ia1.194 Cl (CH₂)₂CH₃ (CH₂)₂—C₆H₅ NH Ia1.195 Cl (CH₂)₃CH₃ (CH₂)₂—C₆H₅ NH Ia1.196 Cl H CH₂CH(CH₃)—C₆H₅ NH Ia1.197 Cl CH₃ CH₂CH(CH₃)—C₆H₅ NH Ia1.198 Cl CH₂CH₃ CH₂CH(CH₃)—C₆H₅ NH Ia1.199 Cl (CH₂)₂CH₃ CH₂CH(CH₃)—C₆H₅ NH Ia1.200 Cl (CH₂)₃CH₃ CH₂CH(CH₃)—C₆H₅ NH Ia1.201 Cl H CH(CH₃)CH₂—C₆H₅ NH Ia1.202 Cl CH₃ CH(CH₃)CH₂—C₆H₅ NH Ia1.203 Cl CH₂CH₃ CH(CH₃)CH₂—C₆H₅ NH Ia1.204 Cl (CH₂)₂CH₃ CH(CH₃)CH₂—C₆H₅ NH Ia1.205 Cl (CH₂)₃CH₃ CH(CH₃)CH₂—C₆H₅ NH Ia1.206 Cl H CH(CH₃)CH(CH₃)—C₆H₅ NH Ia1.207 Cl CH₃ CH(CH₃)CH(CH₃)—C₆H₅ NH Ia1.208 Cl CH₂CH₃ CH(CH₃)CH(CH₃)—C₆H₅ NH Ia1.209 Cl (CH₂)₂CH₃ CH(CH₃)CH(CH₃)—C₆H₅ NH Ia1.210 Cl (CH₂)₃CH₃ CH(CH₃)CH(CH₃)—C₆H₅ NH Ia1.211 Cl H (CH₂)₂-(4-Cl—C₆H₄) NH Ia1.212 Cl CH₃ (CH₂)₂-(4-Cl—C₆H₄) NH Ia1.213 Cl CH₂CH₃ (CH₂)₂-(4-Cl—C₆H₄) NH Ia1.214 Cl (CH₂)₂CH₃ (CH₂)₂-(4-Cl—C₆H₄) NH Ia1.215 Cl (CH₂)₃CH₃ (CH₂)₂-(4-Cl—C₆H₄) NH Ia1.216 Cl H CH₂CH(CH₃)-(4-Cl—C₆H₄) NH Ia1.217 Cl CH₃ CH₂CH(CH₃)-(4-Cl—C₆H₄) NH Ia1.218 Cl CH₂CH₃ CH₂CH(CH₃)-(4-Cl—C₆H₄) Ia1.219 Cl (CH₂)₂CH₃ CH₂CH(CH₃)-(4-Cl—C₆H₄) NH Ia1.220 Cl (CH₂)₃CH₃ CH₂CH(CH₃)-(4-Cl—C₆H₄) NH Ia1.221 Cl H CH(CH₃)CH₂-(4-Cl—C₆H₄) NH Ia1.222 Cl CH₃ CH(CH₃)CH₂-(4-Cl—C₆H₄) NH Ia1.223 Cl CH₂CH₃ CH(CH₃)CH₂-(4-Cl—C₆H₄) NH Ia1.224 Cl (CH₂)₂CH₃ CH(CH₃)CH₂-(4-Cl—C₆H₄) NH Ia1.225 Cl (CH₂)₃CH₃ CH(CH₃)CH₂-(4-Cl—C₆H₄) NH Ia1.226 Cl H CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) NH Ia1.227 Cl CH₃ CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) NH Ia1.228 Cl CH₂CH₃ CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) NH Ia1.229 Cl (CH₂)₂CH₃ CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) NH Ia1.230 Cl (CH₂)₃CH₃ CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) NH Ia1.231 Cl H (CH₂)₂-(2,4-Cl₂—C₆H₃) NH Ia1.232 Cl CH₃ (CH₂)₂-(2,4-Cl₂—C₆H₃) NH Ia1.233 Cl CH₂CH₃ (CH₂)₂-(2,4-Cl₂—C₆H₃) NH Ia1.234 Cl (CH₂)₂CH₃ (CH₂)₂-(2,4-Cl₂—C₆H₃) NH Ia1.235 Cl (CH₂)₃CH₃ (CH₂)₂-(2,4-Cl₂—C₆H₃) NH Ia1.236 Cl H CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) NH Ia1.237 Cl CH₃ CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) NH Ia1.238 Cl CH₂CH₃ CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) NH Ia1.239 Cl (CH₂)₂CH₃ CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) NH Ia1.240 Cl (CH₂)₃CH₃ CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) NH Ia1.241 Cl H CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) NH Ia1.242 Cl CH₃ CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) NH Ia1.243 Cl CH₂CH₃ CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) NH Ia1.244 Cl (CH₂)₂CH₃ CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) NH Ia1.245 Cl (CH₂)₃CH₃ CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) NH Ia1.246 Cl H CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) NH Ia1.247 Cl CH₃ CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) NH Ia1.248 Cl CH₂CH₃ CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) NH Ia1.249 Cl (CH₂)₂CH₃ CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) NH Ia1.250 Cl (CH₂)₃CH₃ CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) NH Ia1.251 Cl H (CH₂)₂—O—C₆H₅ NH Ia1.252 Cl CH₃ (CH₂)₂—O—C₆H₅ NH Ia1.253 Cl CH₂CH₃ (CH₂)₂—O—C₆H₅ NH Ia1.254 Cl (CH₂)₂CH₃ (CH₂)₂—O—C₆H₅ NH Ia1.255 Cl (CH₂)₃CH₃ (CH₂)₂—O—C₆H₅ NH Ia1.256 Cl H CH₂CH(CH₃)—O—C₆H₅ NH Ia1.257 Cl CH₃ CH₂CH(CH₃)—O—C₆H₅ NH Ia1.258 Cl CH₂CH₃ CH₂CH(CH₃)—O—C₆H₅ NH Ia1.259 Cl (CH₂)₂CH₃ CH₂CH(CH₃)—O—C₆H₅ NH Ia1.260 Cl (CH₂)₃CH₃ CH₂CH(CH₃)—O—C₆H₅ NH Ia1.261 Cl H CH(CH₃)CH₂—O—C₆H₅ NH Ia1.262 Cl CH₃ CH(CH₃)CH₂—O—C₆H₅ NH Ia1.263 Cl CH₂CH₃ CH(CH₃)CH₂—O—C₆H₅ NH Ia1.264 Cl (CH₂)₂CH₃ CH(CH₃)CH₂—O—C₆H₅ NH Ia1.265 Cl (CH₂)₃CH₃ CH(CH₃)CH₂—O—C₆H₅ NH Ia1.266 Cl H CH(CH₃)CH(CH₃)—O—C₆H₅ NH Ia1.267 Cl CH₃ CH(CH₃)CH(CH₃)—O—C₆H₅ NH Ia1.268 Cl CH₂CH₃ CH(CH₃)CH(CH₃)—O—C₆H₅ NH Ia1.269 Cl (CH₂)₂CH₃ CH(CH₃)CH(CH₃)—O—C₆H₅ NH Ia1.270 Cl (CH₂)₃CH₃ CH(CH₃)CH(CH₃)—O—C₆H₅ NH Ia1.271 Cl H (CH₂)₂—O-(4-Cl—C₆H₄) NH Ia1.272 Cl CH₃ (CH₂)₂—O-(4-Cl—C₆H₄) NH Ia1.273 Cl CH₂CH₃ (CH₂)₂—O-(4-Cl—C₆H₄) NH Ia1.274 Cl (CH₂)₂CH₃ (CH₂)₂—O-(4-Cl—C₆H₄) NH Ia1.275 Cl (CH₂)₃CH₃ (CH₂)₂—O-(4-Cl—C₆H₄) NH Ia1.276 Cl H CH₂CH(CH₃)—O-(4-Cl—C₆H₄) NH Ia1.277 Cl CH₃ CH₂CH(CH₃)—O-(4-Cl—C₆H₄) NH Ia1.278 Cl CH₂CH₃ CH₂CH(CH₃)—O-(4-Cl—C₆H₄) NH Ia1.279 Cl (CH₂)₂CH₃ CH₂CH(CH₃)—O-(4-Cl—C₆H₄) NH Ia1.280 Cl (CH₂)₃CH₃ CH₂CH(CH₃)—O-(4-Cl—C₆H₄) NH Ia1.281 Cl H CH(CH₃)CH₂—O-(4-Cl—C₆H₄) NH Ia1.282 Cl CH₃ CH(CH₃)CH₂—O-(4-Cl—C₆H₄) NH Ia1.283 Cl CH₂CH₃ CH(CH₃)CH₂—O-(4-Cl—C₆H₄) NH Ia1.284 Cl (CH₂)₂CH₃ CH(CH₃)CH₂—O-(4-Cl—C₆H₄) NH Ia1.285 Cl (CH₂)₃CH₃ CH(CH₃)CH₂—O-(4-Cl—C₆H₄) NH Ia1.286 Cl H CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) NH Ia1.287 Cl CH₃ CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) NH Ia1.288 Cl CH₂CH₃ CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) NH Ia1.289 Cl (CH₂)₂CH₃ CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) NH Ia1.290 Cl (CH₂)₃CH₃ CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) NH Ia1.291 Cl H (CH₂)₂—O-(2,4-Cl₂—C₆H₃) NH Ia1.292 Cl CH₃ (CH₂)₂—O-(2,4-Cl₂—C₆H₃) NH Ia1.293 Cl CH₂CH₃ (CH₂)₂—O-(2 ,4-Cl₂—C₆H₃) NH Ia1.294 Cl (CH₂)₂CH₃ (CH₂)₂—O-(2,4-Cl₂—C₆H₃) NH Ia1.295 Cl (CH₂)₃CH₃ (CH₂)₂—O-(2,4-Cl₂—C₆H₃) NH Ia1.296 Cl H CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NH Ia1.297 Cl CH₃ CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NH Ia1.298 Cl CH₂CH₃ CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NH Ia1.299 Cl (CH₂)₂CH₃ CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NH Ia1.300 Cl (CH₂)₃CH₃ CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NH Ia1.301 Cl H CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) NH Ia1.302 Cl CH₃ CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) NH Ia1.303 Cl CH₂CH₃ CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) NH Ia1.304 Cl (CH₂)₂CH₃ CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) NH Ia1.305 Cl (CH₂)₃CH₃ CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) NH Ia1.306 Cl H CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NH Ia1.307 Cl CH₃ CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NH Ia1.308 Cl CH₂CH₃ CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NH Ia1.309 Cl (CH₂)₂CH₃ CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NH Ia1.310 Cl (CH₂)₃CH₃ CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NH Ia1.311 Cl H CH₃ NCH₃ Ia1.312 Cl CH₃ CH₃ NCH₃ Ia1.313 Cl CH₂CH₃ CH₃ NCH₃ Ia1.314 Cl (CH₂)₂CH₃ CH₃ NCH₃ Ia1.315 Cl (CH₂)₃CH₃ CH₃ NCH₃ Ia1.316 Cl H C₂H₅ NCH₃ Ia1.317 Cl CH₃ C₂H₅ NCH₃ Ia1.318 Cl CH₂CH₃ C₂H₅ NCH₃ Ia1.319 Cl (CH₂)₂CH₃ C₂H₅ NCH₃ Ia1.320 Cl (CH₂)₃CH₃ C₂H₅ NCH₃ Ia1.321 Cl H (CH₂)₂CH₃ NCH₃ Ia1.322 Cl CH₃ (CH₂)₂CH₃ NCH₃ Ia1.323 Cl CH₂CH₃ (CH₂)₂CH₃ NCH₃ Ia1.324 Cl (CH₂)₂CH₃ (CH₂)₂CH₃ NCH₃ Ia1.325 Cl (CH₂)₃CH₃ (CH₂)₂CH₃ NCH₃ Ia1.326 Cl H CH(CH₃)₂ NCH₃ Ia1.327 Cl CH₃ CH(CH₃)₂ NCH₃ Ia1.328 Cl CH₂CH₃ CH(CH₃)₂ NCH₃ Ia1.329 Cl (CH₂)₂CH₃ CH(CH₃)₂ NCH₃ Ia1.330 Cl (CH₂)₃CH₃ CH(CH₃)₂ NCH₃ Ia1.331 Cl H (CH₂)₃CH₃ NCH₃ Ia1.332 Cl CH₃ (CH₂)₃CH₃ NCH₃ Ia1.333 Cl CH₂CH₃ (CH₂)₃CH₃ NCH₃ Ia1.334 Cl (CH₂)₂CH₃ (CH₂)₃CH₃ NCH₃ Ia1.335 Cl (CH₂)₃CH₃ (CH₂)₃CH₃ NCH₃ Ia1.336 Cl H CH₂CH(CH₃)₂ NCH₃ Ia1.337 Cl CH₃ CH₂CH(CH₃)₂ NCH₃ Ia1.338 Cl CH₂CH₃ CH₂CH(CH₃)₂ NCH₃ Ia1.339 Cl (CH₂)₂CH₃ CH₂CH(CH₃)₂ NCH₃ Ia1.340 Cl (CH₂)₃CH₃ CH₂CH(CH₃)₂ NCH₃ Ia1.341 Cl H CH(CH₃)CH₂CH₃ NCH₃ Ia1.342 Cl CH₃ CH(CH₃)CH₂CH₃ NCH₃ Ia1.343 Cl CH₂CH₃ CH(CH₃)CH₂CH₃ NCH₃ Ia1.344 Cl (CH₂)₂CH₃ CH(CH₃)CH₂CH₃ NCH₃ Ia1.345 Cl (CH₂)₃CH₃ CH(CH₃)CH₂CH₃ NCH₃ Ia1.346 Cl H (CH₂)₂—C₆H₅ NCH₃ Ia1.347 Cl CH₃ (CH₂)₂—C₆H₅ NCH₃ Ia1.348 Cl CH₂CH₃ (CH₂)₂—C₆H₅ NCH₃ Ia1.349 Cl (CH₂)₂CH₃ (CH₂)₂—C₆H₅ NCH₃ Ia1.350 Cl (CH₂)₃CH₃ (CH₂)₂—C₆H₅ NCH₃ Ia1.351 Cl H CH₂CH(CH₃)—C₆H₅ NCH₃ Ia1.352 Cl CH₃ CH₂CH(CH₃)—C₆H₅ NCH₃ Ia1.353 Cl CH₂CH₃ CH₂CH(CH₃)—C₆H₅ NCH₃ Ia1.354 Cl (CH₂)₂CH₃ CH₂CH(CH₃)—C₆H₅ NCH₃ Ia1.355 Cl (CH₂)₃CH₃ CH₂CH(CH₃)—C₆H₅ NCH₃ Ia1.356 Cl H CH(CH₃)CH₂—C₆H₅ NCH₃ Ia1.357 Cl CH₃ CH(CH₃)CH₂—C₆H₅ NCH₃ Ia1.358 Cl CH₂CH₃ CH(CH₃)CH₂—C₆H₅ NCH₃ Ia1.359 Cl (CH₂)₂CH₃ CH(CH₃)CH₂—C₆H₅ NCH₃ Ia1.360 Cl (CH₂)₃CH₃ CH(CH₃)CH₂—C₆H₅ NCH₃ Ia1.361 Cl H CH(CH₃)CH(CH₃)—C₆H₅ NCH₃ Ia1.362 Cl CH₃ CH(CH₃)CH(CH₃)—C₆H₅ NCH₃ Ia1.363 Cl CH₂CH₃ CH(CH₃)CH(CH₃)—C₆H₅ NCH₃ Ia1.364 Cl (CH₂)₂CH₃ CH(CH₃)CH(CH₃)—C₆H₅ NCH₃ Ia1.365 Cl (CH2 )₃CH₃ CH(CH₃)CH(CH₃)—C₆H₅ NCH₃ Ia1.366 Cl H (CH₂)₂-(4-Cl—C₆H₄) NCH₃ Ia1.367 Cl CH₃ (CH₂)₂-(4-Cl—C₆H₄) NCH₃ Ia1.368 Cl CH₂CH₃ (CH₂)₂-(4-Cl—C₆H₄) NCH₃ Ia1.369 Cl (CH₂)₂CH₃ (CH₂)₂-(4-Cl—C₆H₄) NCH₃ Ia1.370 Cl (CH₂)₃CH₃ (CH₂)₂-(4-Cl—C₆H₄) NCH₃ Ia1.371 Cl H CH₂CH(CH₃)-(4-Cl—C₆H₄) NCH₃ Ia1.372 Cl CH₃ CH₂CH(CH₃)-(4-Cl—C₆H₄) NCH₃ Ia1.373 Cl CH₂CH₃ CH₂CH(CH₃)-(4-Cl—C₆H₄) NCH₃ Ia1.374 Cl (CH₂)₂CH₃ CH₂CH(CH₃)-(4-Cl—C₆H₄) NCH₃ Ia1.375 Cl (CH₂)₃CH₃ CH₂CH(CH₃)-(4-Cl—C₆H₄) NCH₃ Ia1.376 Cl H CH(CH₃)CH₂-(4-Cl—C₆H₄) NCH₃ Ia1.377 Cl CH₃ CH(CH₃)CH₂-(4-Cl—C₆H₄) NCH₃ Ia1.378 Cl CH₂CH₃ CH(CH₃)CH₂-(4-Cl—C₆H₄) NCH₃ Ia1.379 Cl (CH₂)₂CH₃ CH(CH₃)CH₂-(4-Cl—C₆H₄) NCH₃ Ia1.380 Cl (CH₂)₃CH₃ CH(CH₃)CH₂-(4-Cl—C₆H₄) NCH₃ Ia1.381 Cl H CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) NCH₃ Ia1.382 Cl CH₃ CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) NCH₃ Ia1.383 Cl CH₂CH₃ CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) NCH₃ Ia1.384 Cl (CH₂)₂CH₃ CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) NCH₃ Ia1.385 Cl (CH₂)₃CH₃ CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) NCH₃ Ia1.386 Cl H (CH₂)₂-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.387 Cl CH₃ (CH₂)₂-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.388 Cl CH₂CH₃ (CH₂)₂-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.389 Cl (CH₂)₂CH₃ (CH₂)₂-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.390 Cl (CH₂)₃CH₃ (CH₂)₂-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.391 Cl H CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.392 Cl CH₃ CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.393 Cl CH₂CH₃ CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.394 Cl (CH₂)₂CH₃ CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.395 Cl (CH₂)₃CH₃ CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.396 Cl H CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.397 Cl CH₃ CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.398 Cl CH₂CH₃ CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.399 Cl (CH₂)₂CH₃ CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.400 Cl (CH₂)₃CH₃ CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.401 Cl H CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.402 Cl CH₃ CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.403 Cl CH₂CH₃ CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.404 Cl (CH₂)₂CH₃ CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.405 Cl (CH₂)₃CH₃ CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.406 Cl H (CH₂)₂—O—C₆H₅ NCH₃ Ia1.407 Cl CH₃ (CH₂)₂—O—C₆H₅ NCH₃ Ia1.408 Cl CH₂CH₃ (CH₂)₂—O—C₆H₅ NCH₃ Ia1.409 Cl (CH₂)₂CH₃ (CH₂)₂—O—C₆H₅ NCH₃ Ia1.410 Cl (CH₂)₃CH₃ (CH₂)₂—O—C₆H₅ NCH₃ Ia1.411 Cl H CH₂CH(CH₃)—O—C₆H₅ NCH₃ Ia1.412 Cl CH₃ CH₂CH(CH₃)—O—C₆H₅ NCH₃ Ia1.413 Cl CH₂CH₃ CH₂CH(CH₃)—O—C₆H₅ NCH₃ Ia1.414 Cl (CH₂)₂CH₃ CH₂CH(CH₃)—O—C₆H₅ NCH₃ Ia1.415 Cl (CH₂)₃CH₃ CH₂CH(CH₃)—O—C₆H₅ NCH₃ Ia1.416 Cl H CH(CH₃)CH₂—O—C₆H₅ NCH₃ Ia1.417 Cl CH₃ CH(CH₃)CH₂—O—C₆H₅ NCH₃ Ia1.418 Cl CH₂CH₃ CH(CH₃)CH₂—O—C₆H₅ NCH₃ Ia1.419 Cl (CH₂)₂CH₃ CH(CH₃)CH₂—O—C₆H₅ NCH₃ Ia1.420 Cl (CH₂)₃CH₃ CH(CH₃)CH₂—O—C₆H₅ NCH₃ Ia1.421 Cl H CH(CH₃)CH(CH₃)—O—C₆H₅ NCH₃ Ia1.422 Cl CH₃ CH(CH₃)CH(CH₃)—O—C₆H₅ NCH₃ Ia1.423 Cl CH₂CH₃ CH(CH₃)CH(CH₃)—O—C₆H₅ NCH₃ Ia1.424 Cl (CH₂)₂CH₃ CH(CH₃)CH(CH₃)—O—C₆H₅ NCH₃ Ia1.425 Cl (CH₂)₃CH₃ CH(CH₃)CH(CH₃)—O—C₆H₅ NCH₃ Ia1.426 Cl H (CH₂)₂—O-(4-Cl—C₆H₄) NCH₃ Ia1.427 Cl CH₃ (CH₂)₂—O-(4-Cl—C₆H₄) NCH₃ Ia1.428 Cl CH₂CH₃ (CH₂)₂—O-(4-Cl—C₆H₄) NCH₃ Ia1.429 Cl (CH₂)₂CH₃ (CH₂)₂—O-(4-Cl—C₆H₄) NCH₃ Ia1.430 Cl (CH₂)₃CH₃ (CH₂)₂—O-(4-Cl—C₆H₄) NCH₃ Ia1.431 Cl H CH₂CH(CH₃)—O-(4-Cl—C₆H₄) NCH₃ Ia1.432 Cl CH₃ CH₂CH(CH₃)—O-(4-Cl—C₆H₄) NCH₃ Ia1.433 Cl CH₂CH₃ CH₂CH(CH₃)—O-(4-Cl—C₆H₄) NCH₃ Ia1.434 Cl (CH₂)₂CH₃ CH₂CH(CH₃)—O-(4-Cl—C₆H₄) NCH₃ Ia1.435 Cl (CH₂)₃CH₃ CH₂CH(CH₃)—O-(4-Cl—C₆H₄) NCH₃ Ia1.436 Cl H CH(CH₃)CH₂—O-(4-Cl—C₆H₄) NCH₃ Ia1.437 Cl CH₃ CH(CH₃)CH₂—O-(4-Cl—C₆H₄) NCH₃ Ia1.438 Cl CH₂CH₃ CH(CH₃)CH₂—O-(4-Cl—C₆H₄) NCH₃ Ia1.439 Cl (CH₂)₂CH₃ CH(CH₃)CH₂—O-(4-Cl—C₆H₄) NCH₃ Ia1.440 Cl (CH₂)₃CH₃ CH(CH₃)CH₂—O-(4-Cl—C₆H₄) NCH₃ Ia1.441 Cl H CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) NCH₃ Ia1.442 Cl CH₃ CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) NCH₃ Ia1.443 Cl CH₂CH₃ CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) NCH₃ Ia1.444 Cl (CH₂)₂CH₃ CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) NCH₃ Ia1.445 Cl (CH₂)₃CH₃ CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) NCH₃ Ia1.446 Cl H (CH₂)₂—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.447 Cl CH₃ (CH₂)₂—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.448 Cl CH₂CH₃ (CH₂)₂—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.449 Cl (CH₂)₂CH₃ (CH₂)₂—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.450 Cl (CH₂)₃CH₃ (CH₂)₂—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.451 Cl H CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.452 Cl CH₃ CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.453 Cl CH₂CH₃ CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.454 Cl (CH₂)₂CH₃ CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.455 Cl (CH₂)₃CH₃ CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.456 Cl H CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.457 Cl CH₃ CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.458 Cl CH₂CH₃ CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.459 Cl (CH₂)₂CH₃ CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.460 Cl (CH₂)₃CH₃ CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.461 Cl H CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.462 Cl CH₃ CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.463 Cl CH₂CH₃ CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.464 Cl (CH₂)₂CH₃ CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃₎ NCH₃ Ia1.465 Cl (CH₂)₃CH₃ CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.466 CH₃ H CH₃ O Ia1.467 CH₃ CH₃ CH₃ O Ia1.468 CH₃ CH₂CH₃ CH₃ O Ia1.469 CH₃ (CH₂)₂CH₃ CH₃ O Ia1.470 CH₃ (CH₂)₃CH₃ CH₃ O Ia1.471 CH₃ H C₂H₅ O Ia1.472 CH₃ CH₃ C₂H₅ O Ia1.473 CH₃ CH₂CH₃ C₂H₅ O Ia1.474 CH₃ (CH₂)₂CH₃ C₂H₅ O Ia1.475 CH₃ (CH₂)₃CH₃ C₂H₅ O Ia1.476 CH₃ H (CH₂)₂CH₃ O Ia1.477 CH₃ CH₃ (CH₂)₂CH₃ O Ia1.478 CH₃ CH₂CH₃ (CH₂)₂CH₃ O Ia1.479 CH₃ (CH₂)₂CH₃ (CH₂)₂CH₃ O Ia1.480 CH₃ (CH₂)₃CH₃ (CH₂)₂CH₃ O Ia1.481 CH₃ H CH(CH₃)₂ O Ia1.482 CH₃ CH₃ CH(CH₃)₂ O Ia1.483 CH₃ CH₂CH₃ CH(CH₃)₂ O Ia1.484 CH₃ (CH₂)₂CH₃ CH(CH₃)₂ O Ia1.485 CH₃ (CH₂)₃CH₃ CH(CH₃)₂ O Ia1.486 CH₃ H (CH₂)₃CH₃ O Ia1.487 CH₃ CH₃ (CH₂)₃CH₃ O Ia1.488 CH₃ CH₂CH₃ (CH₂)₃CH₃ O Ia1.489 CH₃ (CH₂)₂CH₃ (CH₂)₃CH₃ O Ia1.490 CH₃ (CH₂)₃CH₃ (CH₂)₃CH₃ O Ia1.491 CH₃ H CH₂CH(CH₃)₂ O Ia1.492 CH₃ CH₃ CH₂CH(CH₃)₂ O Ia1.493 CH₃ CH₂CH₃ CH₂CH(CH₃)₂ O Ia1.494 CH₃ (CH₂)₂CH₃ CH₂CH(CH₃)₂ O Ia1.495 CH₃ (CH₂)₃CH₃ CH₂CH(CH₃)₂ O Ia1.496 CH₃ H CH(CH₃)CH₂CH₃ O Ia1.497 CH₃ CH₃ CH(CH₃)CH₂CH₃ O Ia1.498 CH₃ CH₂CH₃ CH(CH₃)CH₂CH₃ O Ia1.499 CH₃ (CH₂)₂CH₃ CH(CH₃)CH₂CH₃ O Ia1.500 CH₃ (CH₂)₃CH₃ CH(CH₃)CH₂CH₃ O Ia1.501 CH₃ H (CH₂)₂—C₆H₅ O Ia1.502 CH₃ CH₃ (CH₂)₂—C₆H₅ O Ia1.503 CH₃ CH₂CH₃ (CH₂)₂—C₆H₅ O Ia1.504 CH₃ (CH₂)₂CH₃ (CH₂)₂—C₆H₅ O Ia1.505 CH₃ (CH₂)₃CH₃ (CH₂)₂—C₆H₅ O Ia1.506 CH₃ H CH₂CH(CH₃)—C₆H₅ O Ia1.507 CH₃ CH₃ CH₂CH(CH₃)—C₆H₅ O Ia1.508 CH₃ CH₂CH₃ CH₂CH(CH₃)—C₆H₅ O Ia1.509 CH₃ (CH₂)₂CH₃ CH₂CH(CH₃)—C₆H₅ O Ia1.510 CH₃ (CH₂)₃CH₃ CH₂CH(CH₃)—C₆H₅ O Ia1.511 CH₃ H CH(CH₃)CH₂—C₆H₅ O Ia1.512 CH₃ CH₃ CH(CH₃)CH₂—C₆H₅ O Ia1.513 CH₃ CH₂CH₃ CH(CH₃)CH₂—C₆H₅ O Ia1.514 CH₃ (CH₂)₂CH₃ CH(CH₃)CH₂—C₆H₅ O Ia1.515 CH₃ (CH₂)₃CH₃ CH(CH₃)CH₂—C₆H₅ O Ia1.516 CH₃ H CH(CH₃)CH(CH₃)—C₆H₅ O Ia1.517 CH₃ CH₃ CH(CH₃)CH(CH₃)—C₆H₅ O Ia1.518 CH₃ CH₂CH₃ CH(CH₃)CH(CH₃)—C₆H₅ O Ia1.519 CH₃ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)—C₆H₅ O Ia1.520 CH₃ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)—C₆H₅ O Ia1.521 CH₃ H (CH₂)₂-(4-Cl—C₆H₄) O Ia1.522 CH₃ CH₃ (CH₂)₂-(4-Cl—C₆H₄) O Ia1.523 CH₃ CH₂CH₃ (CH₂)₂-(4-Cl—C₆H₄) O Ia1.524 CH₃ (CH₂)₂CH₃ (CH₂)₂-(4-Cl—C₆H₄) O Ia1.525 CH₃ (CH₂)₃CH₃ (CH₂)₂-(4-Cl—C₆H₄) O Ia1.526 CH₃ H CH₂CH(CH₃)-(4-Cl—C₆H₄) O Ia1.527 CH₃ CH₃ CH₂CH(CH₃)-(4-Cl—C₆H₄) O Ia1.528 CH₃ CH₂CH₃ CH₂CH(CH₃)-(4-Cl—C₆H₄) O Ia1.529 CH₃ (CH₂)₂CH₃ CH₂CH(CH₃)-(4-Cl—C₆H₄) O Ia1.530 CH₃ (CH₂)₃CH₃ CH₂CH(CH₃)-(4-Cl—C₆H₄) O Ia1.531 CH₃ H CH(CH₃)CH₂-(4-Cl—C₆H₄) O Ia1.532 CH₃ CH₃ CH(CH₃)CH₂-(4-Cl—C₆H₄) O Ia1.533 CH₃ CH₂CH₃ CH(CH₃)CH₂-(4-Cl—C₆H₄) O Ia1.534 CH₃ (CH₂)₂CH₃ CH(CH₃)CH₂-(4-Cl—C₆H₄) O Ia1.535 CH₃ (CH₂)₃CH₃ CH(CH₃)CH₂-(4-Cl—C₆H₄) O Ia1.536 CH₃ H CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) O Ia1.537 CH₃ CH₃ CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) O Ia1.538 CH₃ CH₂CH₃ CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) O Ia1.539 CH₃ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) O Ia1.540 CH₃ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) O Ia1.541 CH₃ H (CH₂)₂-(2,4-Cl₂—C₆H₃) O Ia1.542 CH₃ CH₃ (CH₂)₂-(2,4-Cl₂—C₆H₃) O Ia1.543 CH₃ CH₂CH₃ (CH₂)₂-(2,4-Cl₂—C₆H₃) O Ia1.544 CH₃ (CH₂)₂CH₃ (CH₂)₂-(2,4-Cl₂—C₆H₃) O Ia1.545 CH₃ (CH₂)₃CH₃ (CH₂)₂-(2,4-Cl₂—C₆H₃) O Ia1.546 CH₃ H CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) O Ia1.547 CH₃ CH₃ CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) O Ia1.548 CH₃ CH₂CH₃ CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) O Ia1.549 CH₃ (CH₂)₂CH₃ CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) O Ia1.550 CH₃ (CH₂)₃CH₃ CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) O Ia1.551 CH₃ H CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) O Ia1.552 CH₃ CH₃ CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) O Ia1.553 CH₃ CH₂CH₃ CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) O Ia1.554 CH₃ (CH₂)₂CH₃ CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) O Ia1.555 CH₃ (CH₂)₃CH₃ CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) O Ia1.556 CH₃ H CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) O Ia1.557 CH₃ CH₃ CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) O Ia1.558 CH₃ CH₂CH₃ CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) O Ia1.559 CH₃ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) O Ia1.560 CH₃ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) O Ia1.561 CH₃ H (CH₂)₂—O—C₆H₅ O Ia1.562 CH₃ CH₃ (CH₂)₂—O—C₆H₅ O Ia1.563 CH₃ CH₂CH₃ (CH₂)₂—O—C₆H₅ O Ia1.564 CH₃ (CH₂)₂CH₃ (CH₂)₂—O—C₆H₅ O Ia1.565 CH₃ (CH₂)₃CH₃ (CH₂)₂—O—C₆H₅ O Ia1.566 CH₃ H CH₂CH(CH₃)—O—C₆H₅ O Ia1.567 CH₃ CH₃ CH₂CH(CH₃)—O—C₆H₅ O Ia1.568 CH₃ CH₂CH₃ CH₂CH(CH₃)—O—C₆H₅ O Ia1.569 CH₃ (CH₂)₂CH₃ CH₂CH(CH₃)—O—C₆H₅ O Ia1.570 CH₃ (CH₂)₃CH₃ CH₂CH(CH₃)—O—C₆H₅ O Ia1.571 CH₃ H CH(CH₃)CH₂—O—C₆H₅ O Ia1.572 CH₃ CH₃ CH(CH₃)CH₂—O—C₆H₅ O Ia1.573 CH₃ CH₂CH₃ CH(CH₃)CH₂—O—C₆H₅ O Ia1.574 CH₃ (CH₂)₂CH₃ CH(CH₃)CH₂—O—C₆H₅ O Ia1.575 CH₃ (CH₂)₃CH₃ CH(CH₃)CH₂—O—C₆H₅ O Ia1.576 CH₃ H CH(CH₃)CH(CH₃)—O—C₆H₅ O Ia1.577 CH₃ CH₃ CH(CH₃)CH(CH₃)—O—C₆H₅ O Ia1.578 CH₃ CH₂CH₃ CH(CH₃)CH(CH₃)—O—C₆H₅ O Ia1.579 CH₃ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)—O—C₆H₅ O Ia1.580 CH₃ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)—O—C₆H₅ O Ia1.581 CH₃ H (CH₂)₂—O-(4-Cl—C₆H₄) O Ia1.582 CH₃ CH₃ (CH₂)₂—O-(4-Cl—C₆H₄) O Ia1.583 CH₃ CH₂CH₃ (CH₂)₂—O-(4-Cl—C₆H₄) O Ia1.584 CH₃ (CH₂)₂CH₃ (CH₂)₂—O-(4-Cl—C₆H₄) O Ia1.585 CH₃ (CH₂)₃CH₃ (CH₂)₂—O-(4-Cl—C₆H₄) O Ia1.586 CH₃ H CH₂CH(CH₃)—O-(4-Cl—C₆H₄) O Ia1.587 CH₃ CH₃ CH₂CH(CH₃)—O-(4-Cl—C₆H₄) O Ia1.588 CH₃ CH₂CH₃ CH₂CH(CH₃)—O-(4-Cl—C₆H₄) O Ia1.589 CH₃ (CH₂)₂CH₃ CH₂CH(CH₃)—O-(4-Cl—C₆H₄) O Ia1.590 CH₃ (CH₂)₃CH₃ CH₂CH(CH₃)—O-(4-Cl—C₆H₄) O Ia1.591 CH₃ H CH(CH₃)CH₂—O-(4-Cl—C₆H₄) O Ia1.592 CH₃ CH₃ CH(CH₃)CH₂—O-(4-Cl—C₆H₄) O Ia1.593 CH₃ CH₂CH₃ CH(CH₃)CH₂—O-(4-Cl—C₆H₄) O Ia1.594 CH₃ (CH₂)₂CH₃ CH(CH₃)CH₂—O-(4-Cl—C₆H₄) O Ia1.595 CH₃ (CH₂)₃CH₃ CH(CH₃)CH₂—O-(4-Cl—C₆H₄) O Ia1.596 CH₃ H CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) O Ia1.597 CH₃ CH₃ CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) O Ia1.598 CH₃ CH₂CH₃ CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) O Ia1.599 CH₃ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) O Ia1.600 CH₃ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) O Ia1.601 CH₃ H (CH₂)₂—O-(2,4-Cl₂—C₆H₃) O Ia1.602 CH₃ CH₃ (CH₂)₂—O-(2,4-Cl₂—C₆H₃) O Ia1.603 CH₃ CH₂CH₃ (CH₂)₂—O-(2,4-Cl₂—C₆H₃) O Ia1.604 CH₃ (CH₂)₂CH₃ (CH₂)₂—O-(2,4-Cl₂—C₆H₃) O Ia1.605 CH₃ (CH₂)₃CH₃ (CH₂)₂—O-(2,4-Cl₂—C₆H₃) O Ia1.606 CH₃ H CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) O Ia1.607 CH₃ CH₃ CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) O Ia1.608 CH₃ CH₂CH₃ CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) O Ia1.609 CH₃ (CH₂)₂CH₃ CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) O Ia1.610 CH₃ (CH₂)₃CH₃ CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) O Ia1.611 CH₃ H CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) O Ia1.612 CH₃ CH₃ CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) O Ia1.613 CH₃ CH₂CH₃ CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) O Ia1.614 CH₃ (CH₂)₂CH₃ CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) O Ia1.615 CH₃ (CH₂)₃CH₃ CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) O Ia1.616 CH₃ H CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) O Ia1.617 CH₃ CH₃ CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) O Ia1.618 CH₃ CH₂CH₃ CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) O Ia1.619 CH₃ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) O Ia1.620 CH₃ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) O Ia1.621 CH₃ H CH₃ NH Ia1.622 CH₃ CH₃ CH₃ NH Ia1.623 CH₃ CH₂CH₃ CH₃ NH Ia1.624 CH₃ (CH₂)₂CH₃ CH₃ NH Ia1.625 CH₃ (CH₂)₃CH₃ CH₃ NH Ia1.626 CH₃ H C₂H₅ NH Ia1.627 CH₃ CH₃ C₂H₅ NH Ia1.628 CH₃ CH₂CH₃ C₂H₅ NH Ia1.629 CH₃ (CH₂)₂CH₃ C₂H₅ NH Ia1.630 CH₃ (CH₂)₃CH₃ C₂H₅ NH Ia1.631 CH₃ H (CH₂)₂CH₃ NH Ia1.632 CH₃ CH₃ (CH₂)₂CH₃ NH Ia1.633 CH₃ CH₂CH₃ (CH₂)₂CH₃ NH Ia1.634 CH₃ (CH₂)₂CH₃ (CH₂)₂CH₃ NH Ia1.635 CH₃ (CH₂)₃CH₃ (CH₂)₂CH₃ NH Ia1.636 CH₃ H CH(CH₃)₂ NH Ia1.637 CH₃ CH₃ CH(CH₃)₂ NH Ia1.638 CH₃ CH₂CH₃ CH(CH₃)₂ NH Ia1.639 CH₃ (CH₂)₂CH₃ CH(CH₃)₂ NH Ia1.640 CH₃ (CH₂)₃CH₃ CH(CH₃)₂ NH Ia1.641 CH₃ H (CH₂)₃CH₃ NH Ia1.642 CH₃ CH₃ (CH₂)₃CH₃ NH Ia1.643 CH₃ CH₂CH₃ (CH₂)₃CH₃ NH Ia1.644 CH₃ (CH₂)₂CH₃ (CH₂)₃CH₃ NH Ia1.645 CH₃ (CH₂)₃CH₃ (CH₂)₃CH₃ NH Ia1.646 CH₃ H CH₂CH(CH₃)₂ NH Ia1.647 CH₃ CH₃ CH₂CH(CH₃)₂ NH Ia1.648 CH₃ CH₂CH₃ CH₂CH(CH₃)₂ NH Ia1.649 CH₃ (CH₂)₂CH₃ CH₂CH(CH₃)₂ NH Ia1.650 CH₃ (CH₂)₃CH₃ CH₂CH(CH₃)₂ NH Ia1.651 CH₃ H CH(CH₃)CH₂CH₃ NH Ia1.652 CH₃ CH₃ CH(CH₃)CH₂CH₃ NH Ia1.653 CH₃ CH₂CH₃ CH(CH₃)CH₂CH₃ NH Ia1.654 CH₃ (CH₂)₂CH₃ CH(CH₃)CH₂CH₃ NH Ia1.655 CH₃ (CH₂)₃CH₃ CH(CH₃)CH₂CH₃ NH Ia1.656 CH₃ H (CH₂)₂—C₆H₅ NH Ia1.657 CH₃ CH₃ (CH₂)₂—C₆H₅ NH Ia1.658 CH₃ CH₂CH₃ (CH₂)₂—C₆H₅ NH Ia1.659 CH₃ (CH₂)₂CH₃ (CH₂)₂—C₆H₅ NH Ia1.660 CH₃ (CH₂)₃CH₃ (CH₂)₂—C₆H₅ NH Ia1.661 CH₃ H CH₂CH(CH₃)—C₆H₅ NH Ia1.662 CH₃ CH₃ CH₂CH(CH₃)—C₆H₅ NH Ia1.663 CH₃ CH₂CH₃ CH₂CH(CH₃)—C₆H₅ NH Ia1.664 CH₃ (CH₂)₂CH₃ CH₂CH(CH₃)—C₆H₅ NH Ia1.665 CH₃ (CH₂)₃CH₃ CH₂CH(CH₃)—C₆H₅ NH Ia1.666 CH₃ H CH(CH₃)CH₂—C₆H₅ NH Ia1.667 CH₃ CH₃ CH(CH₃)CH₂—C₆H₅ NH Ia1.668 CH₃ CH₂CH₃ CH(CH₃)CH₂—C₆H₅ NH Ia1.669 CH₃ (CH₂)₂CH₃ CH(CH₃)CH₂—C₆H₅ NH Ia1.670 CH₃ (CH₂)₃CH₃ CH(CH₃)CH₂—C₆H₅ NH Ia1.671 CH₃ H CH(CH₃)CH(CH₃)—C₆H₅ NH Ia1.672 CH₃ CH₃ CH(CH₃)CH(CH₃)—C₆H₅ NH Ia1.673 CH₃ CH₂CH₃ CH(CH₃)CH(CH₃)—C₆H₅ NH Ia1.674 CH₃ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)—C₆H₅ NH Ia1.675 CH₃ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)—C₆H₅ NH Ia1.676 CH₃ H (CH₂)₂-(4-Cl—C₆H₄) NH Ia1.677 CH₃ CH₃ (CH₂)₂-(4-Cl—C₆H₄) NH Ia1.678 CH₃ CH₂CH₃ (CH₂)₂-(4-Cl—C₆H₄) NH Ia1.679 CH₃ (CH₂)₂CH₃ (CH₂)₂-(4-Cl—C₆H₄) NH Ia1.680 CH₃ (CH₂)₃CH₃ (CH₂)₂-(4-Cl—C₆H₄) NH Ia1.681 CH₃ H CH₂CH(CH₃)-(4-Cl—C₆H₄) NH Ia1.682 CH₃ CH₃ CH₂CH(CH₃)-(4-Cl—C₆H₄) NH Ia1.683 CH₃ CH₂CH₃ CH₂CH(CH₃)-(4-Cl—C₆H₄) NH Ia1.684 CH₃ (CH₂)₂CH₃ CH₂CH(CH₃)-(4-Cl—C₆H₄) NH Ia1.685 CH₃ (CH₂)₃CH₃ CH₂CH(CH₃)-(4-Cl—C₆H₄) NH Ia1.686 CH₃ H CH(CH₃)CH₂-(4-Cl—C₆H₄) NH Ia1.687 CH₃ CH₃ CH(CH₃)CH₂-(4-Cl—C₆H₄) NH Ia1.688 CH₃ CH₂CH₃ CH(CH₃)CH₂-(4-Cl—C₆H₄) NH Ia1.689 CH₃ (CH₂)₂CH₃ CH(CH₃)CH₂-(4-Cl—C₆H₄) NH Ia1.690 CH₃ (CH₂)₃CH₃ CH(CH₃)CH₂-(4-Cl—C₆H₄) NH Ia1.691 CH₃ H CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) NH Ia1.692 CH₃ CH₃ CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) NH Ia1.693 CH₃ CH₂CH₃ CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) NH Ia1.694 CH₃ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) NH Ia1.695 CH₃ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) NH Ia1.696 CH₃ H (CH₂)₂-(2,4-Cl₂—C₆H₃) NH Ia1.697 CH₃ CH₃ (CH₂)₂-(2,4-Cl₂—C₆H₃) NH Ia1.698 CH₃ CH₂CH₃ (CH₂)₂-(2,4-Cl₂—C₆H₃) NH Ia1.699 CH₃ (CH₂)₂CH₃ (CH₂)₂-(2,4-Cl₂—C₆H₃) NH Ia1.700 CH₃ (CH₂)₃CH₃ (CH₂)₂-(2,4-Cl₂—C₆H₃) NH Ia1.701 CH₃ H CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) NH Ia1.702 CH₃ CH₃ CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) NH Ia1.703 CH₃ CH₂CH₃ CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) NH Ia1.704 CH₃ (CH₂)₂CH₃ CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) NH Ia1.705 CH₃ (CH₂)₃CH₃ CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) NH Ia1.706 CH₃ H CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) NH Ia1.707 CH₃ CH₃ CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) NH Ia1.708 CH₃ CH₂CH₃ CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) NH Ia1.709 CH₃ (CH₂)₂CH₃ CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) NH Ia1.710 CH₃ (CH₂)₃CH₃ CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) NH Ia1.711 CH₃ H CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) NH Ia1.712 CH₃ CH₃ CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) NH Ia1.713 CH₃ CH₂CH₃ CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) NH Ia1.714 CH₃ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) NH Ia1.715 CH₃ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) NH Ia1.716 CH₃ H (CH₂)₂—O—C₆H₅ NH Ia1.717 CH₃ CH₃ (CH₂)₂—O—C₆H₅ NH Ia1.718 CH₃ CH₂CH₃ (CH₂)₂—O—C₆H₅ NH Ia1.719 CH₃ (CH₂)₂CH₃ (CH₂)₂—O—C₆H₅ NH Ia1.720 CH₃ (CH₂)₃CH₃ (CH₂)₂—O—C₆H₅ NH Ia1.721 CH₃ H CH₂CH(CH₃)—O—C₆H₅ NH Ia1.722 CH₃ CH₃ CH₂CH(CH₃)—O—C₆H₅ NH Ia1.723 CH₃ CH₂CH₃ CH₂CH(CH₃)—O—C₆H₅ NH Ia1.724 CH₃ (CH₂)₂CH₃ CH₂CH(CH₃)—O—C₆H₅ NH Ia1.725 CH₃ (CH₂)₃CH₃ CH₂CH(CH₃)—O—C₆H₅ NH Ia1.726 CH₃ H CH(CH₃)CH₂—O—C₆H₅ NH Ia1.727 CH₃ CH₃ CH(CH₃)CH₂—O—C₆H₅ NH Ia1.728 CH₃ CH₂CH₃ CH(CH₃)CH₂—O—C₆H₅ NH Ia1.729 CH₃ (CH₂)₂CH₃ CH(CH₃)CH₂—O—C₆H₅ NH Ia1.730 CH₃ (CH₂)₃CH₃ CH(CH₃)CH₂—O—C₆H₅ NH Ia1.731 CH₃ H CH(CH₃)CH(CH₃)—O—C₆H₅ NH Ia1.732 CH₃ CH₃ CH(CH₃)CH(CH₃)—O—C₆H₅ NH Ia1.733 CH₃ CH₂CH₃ CH(CH₃)CH(CH₃)—O—C₆H₅ NH Ia1.734 CH₃ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)—O—C₆H₅ NH Ia1.735 CH₃ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)—O—C₆H₅ NH Ia1.736 CH₃ H (CH₂)₂—O-(4-Cl—C₆H₄) NH Ia1.737 CH₃ CH₃ (CH₂)₂—O-(4-Cl—C₆H₄) NH Ia1.738 CH₃ CH₂CH₃ (CH₂)₂—O-(4-Cl—C₆H₄) NH Ia1.739 CH₃ (CH₂)₂CH₃ (CH₂)₂—O-(4-Cl—C₆H₄) NH Ia1.740 CH₃ (CH₂)₃CH₃ (CH₂)₂—O-(4-Cl—C₆H₄) NH Ia1.741 CH₃ H CH₂CH(CH₃)—O-(4-Cl—C₆H₄) NH Ia1.742 CH₃ CH₃ CH₂CH(CH₃)—O-(4-Cl—C₆H₄) NH Ia1.743 CH₃ CH₂CH₃ CH₂CH(CH₃)—O-(4-Cl—C₆H₄) NH Ia1.744 CH₃ (CH₂)₂CH₃ CH₂CH(CH₃)—O-(4-Cl—C₆H₄) NH Ia1.745 CH₃ (CH₂)₃CH₃ CH₂CH(CH₃)—O-(4-Cl—C₆H₄) NH Ia1.746 CH₃ H CH(CH₃)CH₂—O-(4-Cl—C₆H₄) NH Ia1.747 CH₃ CH₃ CH(CH₃)CH₂—O-(4-Cl—C₆H₄) NH Ia1.748 CH₃ CH₂CH₃ CH(CH₃)CH₂—O-(4-Cl—C₆H₄) NH Ia1.749 CH₃ (CH₂)₂CH₃ CH(CH₃)CH₂—O-(4-Cl—C₆H₄) NH Ia1.750 CH₃ (CH₂)₃CH₃ CH(CH₃)CH₂—O-(4-Cl—C₆H₄) NH Ia1.751 CH₃ H CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) NH Ia1.752 CH₃ CH₃ CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) NH Ia1.753 CH₃ CH₂CH₃ CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) NH Ia1.754 CH₃ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) NH Ia1.755 CH₃ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) NH Ia1.756 CH₃ H (CH₂)₂—O-(2,4-Cl₂—C₆H₃) NH Ia1.757 CH₃ CH₃ (CH₂)₂—O-(2,4-Cl₂—C₆H₃) NH Ia1.758 CH₃ CH₂CH₃ (CH₂)₂—O-(2,4-Cl₂—C₆H₃) NH Ia1.759 CH₃ (CH₂)₂CH₃ (CH₂)₂—O-(2,4-Cl₂—C₆H₃) NH Ia1.760 CH₃ (CH₂)₃CH₃ (CH₂)₂—O-(2,4-Cl₂—C₆H₃) NH Ia1.761 CH₃ H CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NH Ia1.762 CH₃ CH₃ CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NH Ia1.763 CH₃ CH₂CH₃ CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NH Ia1.764 CH₃ (CH₂)₂CH₃ CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NH Ia1.765 CH₃ (CH₂)₃CH₃ CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NH Ia1.766 CH₃ H CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) NH Ia1.767 CH₃ CH₃ CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) NH Ia1.768 CH₃ CH₂CH₃ CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) NH Ia1.769 CH₃ (CH₂)₂CH₃ CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) NH Ia1.770 CH₃ (CH₂)₃CH₃ CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) NH Ia1.771 CH₃ H CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NH Ia1.772 CH₃ CH₃ CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NH Ia1.773 CH₃ CH₂CH₃ CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NH Ia1.774 CH₃ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NH Ia1.775 CH₃ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NH Ia1.776 CH₃ H CH₃ NCH₃ Ia1.777 CH₃ CH₃ CH₃ NCH₃ Ia1.778 CH₃ CH₂CH₃ CH₃ NCH₃ Ia1.779 CH₃ (CH₂)₂CH₃ CH₃ NCH₃ Ia1.780 CH₃ (CH₂)₃CH₃ CH₃ NCH₃ Ia1.781 CH₃ H C₂H₅ NCH₃ Ia1.782 CH₃ CH₃ C₂H₅ NCH₃ Ia1.783 CH₃ CH₂CH₃ C₂H₅ NCH₃ Ia1.784 CH₃ (CH₂)₂CH₃ C₂H₅ NCH₃ Ia1.785 CH₃ (CH₂)₃CH₃ C₂H₅ NCH₃ Ia1.786 CH₃ H (CH₂)₂CH₃ NCH₃ Ia1.787 CH₃ CH₃ (CH₂)₂CH₃ NCH₃ Ia1.788 CH₃ CH₂CH₃ (CH₂)₂CH₃ NCH₃ Ia1.789 CH₃ (CH₂)₂CH₃ (CH₂)₂CH₃ NCH₃ Ia1.790 CH₃ (CH₂)₃CH₃ (CH₂)₂CH₃ NCH₃ Ia1.791 CH₃ H CH(CH₃)₂ NCH₃ Ia1.792 CH₃ CH₃ CH(CH₃)₂ NCH₃ Ia1.793 CH₃ CH₂CH₃ CH(CH₃)₂ NCH₃ Ia1.794 CH₃ (CH₂)₂CH₃ CH(CH₃)₂ NCH₃ Ia1.795 CH₃ (CH₂)₃CH₃ CH(CH₃)₂ NCH₃ Ia1.796 CH₃ H (CH₂)₃CH₃ NCH₃ Ia1.797 CH₃ CH₃ (CH₂)₃CH₃ NCH₃ Ia1.798 CH₃ CH₂CH₃ (CH₂)₃CH₃ NCH₃ Ia1.799 CH₃ (CH₂)₂CH₃ (CH₂)₃CH₃ NCH₃ Ia1.800 CH₃ (CH₂)₃CH₃ (CH₂)₃CH₃ NCH₃ Ia1.801 CH₃ H CH₂CH(CH₃)₂ NCH₃ Ia1.802 CH₃ CH₃ CH₂CH(CH₃)₂ NCH₃ Ia1.803 CH₃ CH₂CH₃ CH₂CH(CH₃)₂ NCH₃ Ia1.804 CH₃ (CH₂)₂CH₃ CH₂CH(CH₃)₂ NCH₃ Ia1.805 CH₃ (CH₂)₃CH₃ CH₂CH(CH₃)₂ NCH₃ Ia1.806 CH₃ H CH(CH₃)CH₂CH₃ NCH₃ Ia1.807 CH₃ CH₃ CH(CH₃)CH₂CH₃ NCH₃ Ia1.808 CH₃ CH₂CH₃ CH(CH₃)CH₂CH₃ NCH₃ Ia1.809 CH₃ (CH₂)₂CH₃ CH(CH₃)CH₂CH₃ NCH₃ Ia1.810 CH₃ (CH₂)₃CH₃ CH(CH₃)CH₂CH₃ NCH₃ Ia1.811 CH₃ H (CH₂)₂—C₆H₅ NCH₃ Ia1.812 CH₃ CH₃ (CH₂)₂—C₆H₅ NCH₃ Ia1.813 CH₃ CH₂CH₃ (CH₂)₂—C₆H₅ NCH₃ Ia1.814 CH₃ (CH₂)₂CH₃ (CH₂)₂—C₆H₅ NCH₃ Ia1.815 CH₃ (CH₂)₃CH₃ (CH₂)₂—C₆H₅ NCH₃ Ia1.816 CH₃ H CH₂CH(CH₃)—C₆H₅ NCH₃ Ia1.817 CH₃ CH₃ CH₂CH(CH₃)—C₆H₅ NCH₃ Ia1.818 CH₃ CH₂CH₃ CH₂CH(CH₃)—C₆H₅ NCH₃ Ia1.819 CH₃ (CH₂)₂CH₃ CH₂CH(CH₃)—C₆H₅ NCH₃ Ia1.820 CH₃ (CH₂)₃CH₃ CH₂CH(CH₃)—C₆H₅ NCH₃ Ia1.821 CH₃ H CH(CH₃)CH₂—C₆H₅ NCH₃ Ia1.822 CH₃ CH₃ CH(CH₃)CH₂—C₆H₅ NCH₃ Ia1.823 CH₃ CH₂CH₃ CH(CH₃)CH₂—C₆H₅ NCH₃ Ia1.824 CH₃ (CH₂)₂CH₃ CH(CH₃)CH₂—C₆H₅ NCH₃ Ia1.825 CH₃ (CH₂)₃CH₃ CH(CH₃)CH₂—C₆H₅ NCH₃ Ia1.826 CH₃ H CH(CH₃)CH(CH₃)—C₆H₅ NCH₃ Ia1.827 CH₃ CH₃ CH(CH₃)CH(CH₃)—C₆H₅ NCH₃ Ia1.828 CH₃ CH₂CH₃ CH(CH₃)CH(CH₃)—C₆H₅ NCH₃ Ia1.829 CH₃ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)—C₆H₅ NCH₃ Ia1.830 CH₃ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)—C₆H₅ NCH₃ Ia1.831 CH₃ H (CH₂)₂-(4-Cl—C₆H₄) NCH₃ Ia1.832 CH₃ CH₃ (CH₂)₂-(4-Cl—C₆H₄) NCH₃ Ia1.833 CH₃ CH₂CH₃ (CH₂)₂-(4-Cl—C₆H₄) NCH₃ Ia1.834 CH₃ (CH₂)₂CH₃ (CH₂)₂-(4-Cl—C₆H₄) NCH₃ Ia1.835 CH₃ (CH₂)₃CH₃ (CH₂)₂-(4-Cl—C₆H₄) NCH₃ Ia1.836 CH₃ H CH₂CH(CH₃)-(4-Cl—C₆H₄) NCH₃ Ia1.837 CH₃ CH₃ CH₂CH(CH₃)-(4-Cl—C₆H₄) NCH₃ Ia1.838 CH₃ CH₂CH₃ CH₂CH(CH₃)-(4-Cl—C₆H₄) NCH₃ Ia1.839 CH₃ (CH₂)₂CH₃ CH₂CH(CH₃)-(4-Cl—C₆H₄) NCH₃ Ia1.840 CH₃ (CH₂)₃CH₃ CH₂CH(CH₃)-(4-Cl—C₆H₄) NCH₃ Ia1.841 CH₃ H CH(CH₃)CH₂-(4-Cl—C₆H₄) NCH₃ Ia1.842 CH₃ CH₃ CH(CH₃)CH₂-(4-Cl—C₆H₄) NCH₃ Ia1.843 CH₃ CH₂CH₃ CH(CH₃)CH₂-(4-Cl—C₆H₄) NCH₃ Ia1.844 CH₃ (CH₂)₂CH₃ CH(CH₃)CH₂-(4-Cl—C₆H₄) NCH₃ Ia1.845 CH₃ (CH₂)₃CH₃ CH(CH₃)CH₂-(4-Cl—C₆H₄) NCH₃ Ia1.846 CH₃ H CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) NCH₃ Ia1.847 CH₃ CH₃ CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) NCH₃ Ia1.848 CH₃ CH₂CH₃ CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) NCH₃ Ia1.849 CH₃ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) NCH₃ Ia1.850 CH₃ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) NCH₃ Ia1.851 CH₃ H (CH₂)₂-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.852 CH₃ CH₃ (CH₂)₂-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.853 CH₃ CH₂CH₃ (CH₂)₂-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.854 CH₃ (CH₂)₂CH₃ (CH₂)₂-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.855 CH₃ (CH₂)₃CH₃ (CH₂)₂-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.856 CH₃ H CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.857 CH₃ CH₃ CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.858 CH₃ CH₂CH₃ CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.859 CH₃ (CH₂)₂CH₃ CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.860 CH₃ (CH₂)₃CH₃ CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.861 CH₃ H CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.862 CH₃ CH₃ CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.863 CH₃ CH₂CH₃ CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.864 CH₃ (CH₂)₂CH₃ CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.865 CH₃ (CH₂)₃CH₃ CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.866 CH₃ H CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.867 CH₃ CH₃ CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.868 CH₃ CH₂CH₃ CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.869 CH₃ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.870 CH₃ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.871 CH₃ H (CH₂)₂—O—C₆H₅ NCH₃ Ia1.872 CH₃ CH₃ (CH₂)₂—O—C₆H₅ NCH₃ Ia1.873 CH₃ CH₂CH₃ (CH₂)₂—O—C₆H₅ NCH₃ Ia1.874 CH₃ (CH₂)₂CH₃ (CH₂)₂—O—C₆H₅ NCH₃ Ia1.875 CH₃ (CH₂)₃CH₃ (CH₂)₂—O—C₆H₅ NCH₃ Ia1.876 CH₃ H CH₂CH(CH₃)—O—C₆H₅ NCH₃ Ia1.877 CH₃ CH₃ CH₂CH(CH₃)—O—C₆H₅ NCH₃ Ia1.878 CH₃ CH₂CH₃ CH₂CH(CH₃)—O—C₆H₅ NCH₃ Ia1.879 CH₃ (CH₂)₂CH₃ CH₂CH(CH₃)—O—C₆H₅ NCH₃ Ia1.880 CH₃ (CH₂)₃CH₃ CH₂CH(CH₃)—O—C₆H₅ NCH₃ Ia1.881 CH₃ H CH(CH₃)CH₂—O—C₆H₅ NCH₃ Ia1.882 CH₃ CH₃ CH(CH₃)CH₂—O—C₆H₅ NCH₃ Ia1.883 CH₃ CH₂CH₃ CH(CH₃)CH₂—O—C₆H₅ NCH₃ Ia1.884 CH₃ (CH₂)₂CH₃ CH(CH₃)CH₂—O—C₆H₅ NCH₃ Ia1.885 CH₃ (CH₂)₃CH₃ CH(CH₃)CH₂—O—C₆H₅ NCH₃ Ia1.886 CH₃ H CH(CH₃)CH(CH₃)—O—C₆H₅ NCH₃ Ia1.887 CH₃ CH₃ CH(CH₃)CH(CH₃)—O—C₆H₅ NCH₃ Ia1.888 CH₃ CH₂CH₃ CH(CH₃)CH(CH₃)—O—C₆H₅ NCH₃ Ia1.889 CH₃ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)—O—C₆H₅ NCH₃ Ia1.890 CH₃ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)—O—C₆H₅ NCH₃ Ia1.891 CH₃ H (CH₂)₂—O-(4-Cl—C₆H₄) NCH₃ Ia1.892 CH₃ CH₃ (CH₂)₂—O-(4-Cl—C₆H₄) NCH₃ Ia1.893 CH₃ CH₂CH₃ (CH₂)₂—O-(4-Cl—C₆H₄) NCH₃ Ia1.894 CH₃ (CH₂)₂CH₃ (CH₂)₂—O-(4-Cl—C₆H₄) NCH₃ Ia1.895 CH₃ (CH₂)₃CH₃ (CH₂)₂—O-(4-Cl—C₆H₄) NCH₃ Ia1.896 CH₃ H CH₂CH(CH₃)—O-(4-Cl—C₆H₄) NCH₃ Ia1.897 CH₃ CH₃ CH₂CH(CH₃)—O-(4-Cl—C₆H₄) NCH₃ Ia1.898 CH₃ CH₂CH₃ CH₂CH(CH₃)—O-(4-Cl—C₆H₄) NCH₃ Ia1.899 CH₃ (CH₂)₂CH₃ CH₂CH(CH₃)—O-(4-Cl—C₆H₄) NCH₃ Ia1.900 CH₃ (CH₂)₃CH₃ CH₂CH(CH₃)—O-(4-Cl—C₆H₄) NCH₃ Ia1.901 CH₃ H CH(CH₃)CH₂—O-(4-Cl—C₆H₄) NCH₃ Ia1.902 CH₃ CH₃ CH(CH₃)CH₂—O-(4-Cl—C₆H₄) NCH₃ Ia1.903 CH₃ CH₂CH₃ CH(CH₃)CH₂—O-(4-Cl—C₆H₄) NCH₃ Ia1.904 CH₃ (CH₂)₂CH₃ CH(CH₃)CH₂—O-(4-Cl—C₆H₄) NCH₃ Ia1.905 CH₃ (CH₂)₃CH₃ CH(CH₃)CH₂—O-(4-Cl—C₆H₄) NCH₃ Ia1.906 CH₃ H CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) NCH₃ Ia1.907 CH₃ CH₃ CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) NCH₃ Ia1.908 CH₃ CH₂CH₃ CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) NCH₃ Ia1.909 CH₃ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) NCH₃ Ia1.910 CH₃ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) NCH₃ Ia1.911 CH₃ H (CH₂)₂—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.912 CH₃ CH₃ (CH₂)₂—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.913 CH₃ CH₂CH₃ (CH₂)₂—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.914 CH₃ (CH₂)₂CH₃ (CH₂)₂—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.915 CH₃ (CH₂)₃CH₃ (CH₂)₂—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.916 CH₃ H CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.917 CH₃ CH₃ CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.918 CH₃ CH₂CH₃ CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.919 CH₃ (CH₂)₂CH₃ CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.920 CH₃ (CH₂)₃CH₃ CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.921 CH₃ H CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.922 CH₃ CH₃ CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.923 CH₃ CH₂CH₃ CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.924 CH₃ (CH₂)₂CH₃ CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.925 CH₃ (CH₂)₃CH₃ CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.926 CH₃ H CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.927 CH₃ CH₃ CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.928 CH₃ CH₂CH₃ CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.929 CH₃ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.930 CH₃ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.931 OCH₃ H CH₃ O Ia1.932 OCH₃ CH₃ CH₃ O Ia1.933 OCH₃ CH₂CH₃ CH₃ O Ia1.934 OCH₃ (CH₂)₂CH₃ CH₃ O Ia1.935 OCH₃ (CH₂)₃CH₃ CH₃ O Ia1.936 OCH₃ H C₂H₅ O Ia1.937 OCH₃ CH₃ C₂H₅ O Ia1.938 OCH₃ CH₂CH₃ C₂H₅ O Ia1.939 OCH₃ (CH₂)₂CH₃ C₂H₅ O Ia1.940 OCH₃ (CH₂)₃CH₃ C₂H₅ O Ia1.941 OCH₃ H (CH₂)₂CH₃ O Ia1.942 OCH₃ CH₃ (CH₂)₂CH₃ O Ia1.943 OCH₃ CH₂CH₃ (CH₂)₂CH₃ O Ia1.944 OCH₃ (CH₂)₂CH₃ (CH₂)₂CH₃ O Ia1.945 OCH₃ (CH₂)₃CH₃ (CH₂)₂CH₃ O Ia1.946 OCH₃ H CH(CH₃)₂ O Ia1.947 OCH₃ CH₃ CH(CH₃)₂ O Ia1.948 OCH₃ CH₂CH₃ CH(CH₃)₂ O Ia1.949 OCH₃ (CH₂)₂CH₃ CH(CH₃)₂ O Ia1.950 OCH₃ (CH₂)₃CH₃ CH(CH₃)₂ O Ia1.951 OCH₃ H (CH₂)₃CH₃ O Ia1.952 OCH₃ CH₃ (CH₂)₃CH₃ O Ia1.953 OCH₃ CH₂CH₃ (CH₂)₃CH₃ O Ia1.954 OCH₃ (CH₂)₂CH₃ (CH₂)₃CH₃ O Ia1.955 OCH₃ (CH₂)₃CH₃ (CH₂)₃CH₃ O Ia1.956 OCH₃ H CH₂CH(CH₃)₂ O Ia1.957 OCH₃ CH₃ CH₂CH(CH₃)₂ O Ia1.958 OCH₃ CH₂CH₃ CH₂CH(CH₃)₂ O Ia1.959 OCH₃ (CH₂)₂CH₃ CH₂CH(CH₃)₂ O Ia1.960 OCH₃ (CH₂)₃CH₃ CH₂CH(CH₃)₂ O Ia1.961 OCH₃ H CH(CH₃)CH₂CH₃ O Ia1.962 OCH₃ CH₃ CH(CH₃)CH₂CH₃ O Ia1.963 OCH₃ CH₂CH₃ CH(CH₃)CH₂CH₃ O Ia1.964 OCH₃ (CH₂)₂CH₃ CH(CH₃)CH₂CH₃ O Ia1.965 OCH₃ (CH₂)₃CH₃ CH(CH₃)CH₂CH₃ O Ia1.966 OCH₃ H (CH₂)₂—C₆H₅ O Ia1.967 OCH₃ CH₃ (CH₂)₂—C₆H₅ O Ia1.968 OCH₃ CH₂CH₃ (CH₂)₂—C₆H₅ O Ia1.969 OCH₃ (CH₂)₂CH₃ (CH₂)₂—C₆H₅ O Ia1.970 OCH₃ (CH₂)₃CH₃ (CH₂)₂—C₆H₅ O Ia1.971 OCH₃ H CH₂CH(CH₃)—C₆H₅ O Ia1.972 OCH₃ CH₃ CH₂CH(CH₃)—C₆H₅ O Ia1.973 OCH₃ CH₂CH₃ CH₂CH(CH₃)—C₆H₅ O Ia1.974 OCH₃ (CH₂)₂CH₃ CH₂CH(CH₃)—C₆H₅ O Ia1.975 OCH₃ (CH₂)₃CH₃ CH₂CH(CH₃)—C₆H₅ O Ia1.976 OCH₃ H CH(CH₃)CH₂—C₆H₅ O Ia1.977 OCH₃ CH₃ CH(CH₃)CH₂—C₆H₅ O Ia1.978 OCH₃ CH₂CH₃ CH(CH₃)CH₂—C₆H₅ O Ia1.979 OCH₃ (CH₂)₂CH₃ CH(CH₃)CH₂—C₆H₅ O Ia1.980 OCH₃ (CH₂)₃CH₃ CH(CH₃)CH₂—C₆H₅ O Ia1.981 OCH₃ H CH(CH₃)CH(CH₃)—C₆H₅ O Ia1.982 OCH₃ CH₃ CH(CH₃)CH(CH₃)—C₆H₅ O Ia1.983 OCH₃ CH₂CH₃ CH(CH₃)CH(CH₃)—C₆H₅ O Ia1.984 OCH₃ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)—C₆H₅ O Ia1.985 OCH₃ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)—C₆H₅ O Ia1.986 OCH₃ H (CH₂)₂-(4-Cl—C₆H₄) O Ia1.987 OCH₃ CH₃ (CH₂)₂-(4-Cl—C₆H₄) O Ia1.988 OCH₃ CH₂CH₃ (CH₂)₂-(4-Cl—C₆H₄) O Ia1.989 OCH₃ (CH₂)₂CH₃ (CH₂)₂-(4-Cl—C₆H₄) O Ia1.990 OCH₃ (CH₂)₃CH₃ (CH₂)₂-(4-Cl—C₆H₄) O Ia1.991 OCH₃ H CH₂CH(CH₃)-(4-Cl—C₆H₄) O Ia1.992 OCH₃ CH₃ CH₂CH(CH₃)-(4-Cl—C₆H₄) O Ia1.993 OCH₃ CH₂CH₃ CH₂CH(CH₃)-(4-Cl—C₆H₄) O Ia1.994 OCH₃ (CH₂)₂CH₃ CH₂CH(CH₃)-(4-Cl—C₆H₄) O Ia1.995 OCH₃ (CH₂)₃CH₃ CH₂CH(CH₃)-(4-Cl—C₆H₄) O Ia1.996 OCH₃ H CH(CH₃)CH₂-(4-Cl—C₆H₄) O Ia1.997 OCH₃ CH₃ CH(CH₃)CH₂-(4-Cl—C₆H₄) O Ia1.998 OCH₃ CH₂CH₃ CH(CH₃)CH₂-(4-Cl—C₆H₄) O Ia1.999 OCH₃ (CH₂)₂CH₃ CH(CH₃)CH₂-(4-Cl—C₆H₄) O Ia1.1000 OCH₃ (CH₂)₃CH₃ CH(CH₃)CH₂-(4-Cl—C₆H₄) O Ia1.1001 OCH₃ H CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) O Ia1.1002 OCH₃ CH₃ CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) O Ia1.1003 OCH₃ CH₂CH₃ CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) O Ia1.1004 OCH₃ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) O Ia1.1005 OCH₃ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) O Ia1.1006 OCH₃ H (CH₂)₂-(2,4-Cl₂—C₆H₃) O Ia1.1007 OCH₃ CH₃ (CH₂)₂-(2,4-Cl₂—C₆H₃) O Ia1.1008 OCH₃ CH₂CH₃ (CH₂)₂-(2,4-Cl₂—C₆H₃) O Ia1.1009 OCH₃ (CH₂)₂CH₃ (CH₂)₂-(2,4-Cl₂—C₆H₃) O Ia1.1010 OCH₃ (CH₂)₃CH₃ (CH₂)₂-(2,4-Cl₂—C₆H₃) O Ia1.1011 OCH₃ H CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) O Ia1.1012 OCH₃ CH₃ CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) O Ia1.1013 OCH₃ CH₂CH₃ CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) O Ia1.1014 OCH₃ (CH₂)₂CH₃ CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) O Ia1.1015 OCH₃ (CH₂)₃CH₃ CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) O Ia1.1016 OCH₃ H CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) O Ia1.1017 OCH₃ CH₃ CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) O Ia1.1018 OCH₃ CH₂CH₃ CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) O Ia1.1019 OCH₃ (CH₂)₂CH₃ CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) O Ia1.1020 OCH₃ (CH₂)₃CH₃ CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) O Ia1.1021 OCH₃ H CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) O Ia1.1022 OCH₃ CH₃ CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) O Ia1.1023 OCH₃ CH₂CH₃ CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) O Ia1.1024 OCH₃ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) O Ia1.1025 OCH₃ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) O Ia1.1026 OCH₃ H (CH₂)₂—O—C₆H₅ O Ia1.1027 OCH₃ CH₃ (CH₂)₂—O—C₆H₅ O Ia1.1028 OCH₃ CH₂CH₃ (CH₂)₂—O—C₆H₅ O Ia1.1029 OCH₃ (CH₂)₂CH₃ (CH₂)₂—O—C₆H₅ O Ia1.1030 OCH₃ (CH₂)₃CH₃ (CH₂)₂—O—C₆H₅ O Ia1.1031 OCH₃ H CH₂CH(CH₃)—O—C₆H₅ O Ia1.1032 OCH₃ CH₃ CH₂CH(CH₃)—O—C₆H₅ O Ia1.1033 OCH₃ CH₂CH₃ CH₂CH(CH₃)—O—C₆H₅ O Ia1.1034 OCH₃ (CH₂)₂CH₃ CH₂CH(CH₃)—O—C₆H₅ O Ia1.1035 OCH₃ (CH₂)₃CH₃ CH₂CH(CH₃)—O—C₆H₅ O Ia1.1036 OCH₃ H CH(CH₃)CH₂—O—C₆H₅ O Ia1.1037 OCH₃ CH₃ CH(CH₃)CH₂—O—C₆H₅ O Ia1.1038 OCH₃ CH₂CH₃ CH(CH₃)CH₂—O—C₆H₅ O Ia1.1039 OCH₃ (CH₂)₂CH₃ CH(CH₃)CH₂—O—C₆H₅ O Ia1.1040 OCH₃ (CH₂)₃CH₃ CH(CH₃)CH₂—O—C₆H₅ O Ia1.1041 OCH₃ H CH(CH₃)CH(CH₃)—O—C₆H₅ O Ia1.1042 OCH₃ CH₃ CH(CH₃)CH(CH₃)—O—C₆H₅ O Ia1.1043 OCH₃ CH₂CH₃ CH(CH₃)CH(CH₃)—O—C₆H₅ O Ia1.1044 OCH₃ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)—O—C₆H₅ O Ia1.1045 OCH₃ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)—O—C₆H₅ O Ia1.1046 OCH₃ H (CH₂)₂—O-(4-Cl—C₆H₄) O Ia1.1047 OCH₃ CH₃ (CH₂)₂—O-(4-Cl—C₆H₄) O Ia1.1048 OCH₃ CH₂CH₃ (CH₂)₂—O-(4-Cl—C₆H₄) O Ia1.1049 OCH₃ (CH₂)₂CH₃ (CH₂)₂—O-(4-Cl—C₆H₄) O Ia1.1050 OCH₃ (CH₂)₃CH₃ (CH₂)₂—O-(4-Cl—C₆H₄) O Ia1.1051 OCH₃ H CH₂CH(CH₃)—O-(4-Cl—C₆H₄) O Ia1.1052 OCH₃ CH₃ CH₂CH(CH₃)—O-(4-Cl—C₆H₄) O Ia1.1053 OCH₃ CH₂CH₃ CH₂CH(CH₃)—O-(4-Cl—C₆H₄) O Ia1.1054 OCH₃ (CH₂)₂CH₃ CH₂CH(CH₃)—O-(4-Cl—C₆H₄) O Ia1.1055 OCH₃ (CH₂)₃CH₃ CH₂CH(CH₃)—O-(4-Cl—C₆H₄) O Ia1.1056 OCH₃ H CH(CH₃)CH₂—O-(4-Cl—C₆H₄) O Ia1.1057 OCH₃ CH₃ CH(CH₃)CH₂—O-(4-Cl—C₆H₄) O Ia1.1058 OCH₃ CH₂CH₃ CH(CH₃)CH₂—O-(4-Cl—C₆H₄) O Ia1.1059 OCH₃ (CH₂)₂CH₃ CH(CH₃)CH₂—O-(4-Cl—C₆H₄) O Ia1.1060 OCH₃ (CH₂)₃CH₃ CH(CH₃)CH₂—O-(4-Cl—C₆H₄) O Ia1.1061 OCH₃ H CH(CH₃)CH(CH₃)-O-(4-Cl—C₆H₄) O Ia1.1062 OCH₃ CH₃ CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) O Ia1.1063 OCH₃ CH₂CH₃ CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) O Ia1.1064 OCH₃ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) O Ia1.1065 OCH₃ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) O Ia1.1066 OCH₃ H (CH₂)₂—O-(2,4-Cl₂—C₆H₃) O Ia1.1067 OCH₃ CH₃ (CH₂)₂—O-(2,4-Cl₂—C₆H₃) O Ia1.1068 OCH₃ CH₂CH₃ (CH₂)₂—O-(2,4-Cl₂—C₆H₃) O Ia1.1069 OCH₃ (CH₂)₂CH₃ (CH₂)₂—O-(2,4-Cl₂—C₆H₃) O Ia1.1070 OCH₃ (CH₂)₃CH₃ (CH₂)₂—O-(2,4-Cl₂—C₆H₃) O Ia1.1071 OCH₃ H CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) O Ia1.1072 OCH₃ CH₃ CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) O Ia1.1073 OCH₃ CH₂CH₃ CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) O Ia1.1074 OCH₃ (CH₂)₂CH₃ CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) O Ia1.1075 OCH₃ (CH₂)₃CH₃ CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) O Ia1.1076 OCH₃ H CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) O Ia1.1077 OCH₃ CH₃ CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) O Ia1.1078 OCH₃ CH₂CH₃ CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) O Ia1.1079 OCH₃ (CH₂)₂CH₃ CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) O Ia1.1080 OCH₃ (CH₂)₃CH₃ CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) O Ia1.1081 OCH₃ H CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) O Ia1.1082 OCH₃ CH₃ CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) O Ia1.1083 OCH₃ CH₂CH₃ CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) O Ia1.1084 OCH₃ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) O Ia1.1085 OCH₃ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) O Ia1.1086 OCH₃ H CH₃ NH Ia1.1087 OCH₃ CH₃ CH₃ NH Ia1.1088 OCH₃ CH₂CH₃ CH₃ NH Ia1.1089 OCH₃ (CH₂)₂CH₃ CH₃ NH Ia1.1090 OCH₃ (CH₂)₃CH₃ CH₃ NH Ia1.1091 OCH₃ H C₂H₅ NH Ia1.1092 OCH₃ CH₃ C₂H₅ NH Ia1.1093 OCH₃ CH₂CH₃ C₂H₅ NH Ia1.1094 OCH₃ (CH₂)₂CH₃ C₂H₅ NH Ia1.1095 OCH₃ (CH₂)₃CH₃ C₂H₅ NH Ia1.1096 OCH₃ H (CH₂)₂CH₃ NH Ia1.1097 OCH₃ CH₃ (CH₂)₂CH₃ NH Ia1.1098 OCH₃ CH₂CH₃ (CH₂)₂CH₃ NH Ia1.1099 OCH₃ (CH₂)₂CH₃ (CH₂)₂CH₃ NH Ia1.1100 OCH₃ (CH₂)₃CH₃ (CH₂)₂CH₃ NH Ia1.1101 OCH₃ H CH(CH₃)₂ NH Ia1.1102 OCH₃ CH₃ CH(CH₃)₂ NH Ia1.1103 OCH₃ CH₂CH₃ CH(CH₃)₂ NH Ia1.1104 OCH₃ (CH₂)₂CH₃ CH(CH₃)₂ NH Ia1.1105 OCH₃ (CH₂)₃CH₃ CH(CH₃)₂ NH Ia1.1106 OCH₃ H (CH₂)₃CH₃ NH Ia1.1107 OCH₃ CH₃ (CH₂)₃CH₃ NH Ia1.1108 OCH₃ CH₂CH₃ (CH₂)₃CH₃ NH Ia1.1109 OCH₃ (CH₂)₂CH₃ (CH₂)₃CH₃ NH Ia1.1110 OCH₃ (CH₂)₃CH₃ (CH₂)₃CH₃ NH Ia1.1111 OCH₃ H CH₂CH(CH₃)₂ NH Ia1.1112 OCH₃ CH₃ CH₂CH(CH₃)₂ NH Ia1.1113 OCH₃ CH₂CH₃ CH₂CH(CH₃)₂ NH Ia1.1114 OCH₃ (CH₂)₂CH₃ CH₂CH(CH₃)₂ NH Ia1.1115 OCH₃ (CH₂)₃CH₃ CH₂CH(CH₃)₂ NH Ia1.1116 OCH₃ H CH(CH₃)CH₂CH₃ NH Ia1.1117 OCH₃ CH₃ CH(CH₃)CH₂CH₃ NH Ia1.1118 OCH₃ CH₂CH₃ CH(CH₃)CH₂CH₃ NH Ia1.1119 OCH₃ (CH₂)₂CH₃ CH(CH₃)CH₂CH₃ NH Ia1.1120 OCH₃ (CH₂)₃CH₃ CH(CH₃)CH₂CH₃ NH Ia1.1121 OCH₃ H (CH₂)₂—C₆H₅ NH Ia1.1122 OCH₃ CH₃ (CH₂)₂—C₆H₅ NH Ia1.1123 OCH₃ CH₂CH₃ (CH₂)₂—C₆H₅ NH Ia1.1124 OCH₃ (CH₂)₂CH₃ (CH₂)₂—C₆H₅ NH Ia1.1125 OCH₃ (CH₂)₃CH₃ (CH₂)₂—C₆H₅ NH Ia1.1126 OCH₃ H CH₂CH(CH₃)—C₆H₅ NH Ia1.1127 OCH₃ CH₃ CH₂CH(CH₃)—C₆H₅ NH Ia1.1128 OCH₃ CH₂CH₃ CH₂CH(CH₃)—C₆H₅ NH Ia1.1129 OCH₃ (CH₂)₂CH₃ CH₂CH(CH₃)—C₆H₅ NH Ia1.1130 OCH₃ (CH₂)₃CH₃ CH₂CH(CH₃)—C₆H₅ NH Ia1.1131 OCH₃ H CH(CH₃)CH₂—C₆H₅ NH Ia1.1132 OCH₃ CH₃ CH(CH₃)CH₂—C₆H₅ NH Ia1.1133 OCH₃ CH₂CH₃ CH(CH₃)CH₂—C₆H₅ NH Ia1.1134 OCH₃ (CH₂)₂CH₃ CH(CH₃)CH₂—C₆H₅ NH Ia1.1135 OCH₃ (CH₂)₃CH₃ CH(CH₃)CH₂—C₆H₅ NH Ia1.1136 OCH₃ H CH(CH₃)CH(CH₃)—C₆H₅ NH Ia1.1137 OCH₃ CH₃ CH(CH₃)CH(CH₃)—C₆H₅ NH Ia1.1138 OCH₃ CH₂CH₃ CH(CH₃)CH(CH₃)—C₆H₅ NH Ia1.1139 OCH₃ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)—C₆H₅ NH Ia1.1140 OCH₃ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)—C₆H₅ NH Ia1.1141 OCH₃ H (CH₂)₂-(4-Cl—C₆H₄) NH Ia1.1142 OCH₃ CH₃ (CH₂)₂-(4-Cl—C₆H₄) NH Ia1.1143 OCH₃ CH₂CH₃ (CH₂)₂-(4-Cl—C₆H₄) NH Ia1.1144 OCH₃ (CH₂)₂CH₃ (CH₂)₂-(4-Cl—C₆H₄) NH Ia1.1145 OCH₃ (CH₂)₃CH₃ (CH₂)₂-(4-Cl—C₆H₄) NH Ia1.1146 OCH₃ H CH₂CH(CH₃)-(4-Cl—C₆H₄) NH Ia1.1147 OCH₃ CH₃ CH₂CH(CH₃)-(4-Cl—C₆H₄) NH Ia1.1148 OCH₃ CH₂CH₃ CH₂CH(CH₃)-(4-Cl—C₆H₄) NH Ia1.1149 OCH₃ (CH₂)₂CH₃ CH₂CH(CH₃)-(4-Cl—C₆H₄) NH Ia1.1150 OCH₃ (CH₂)₃CH₃ CH₂CH(CH₃)-(4-Cl—C₆H₄) NH Ia1.1151 OCH₃ H CH(CH₃)CH₂-(4-Cl—C₆H₄) NH Ia1.1152 OCH₃ CH₃ CH(CH₃)CH₂-(4-Cl—C₆H₄) NH Ia1.1153 OCH₃ CH₂CH₃ CH(CH₃)CH₂-(4-Cl—C₆H₄) NH Ia1.1154 OCH₃ (CH₂)₂CH₃ CH(CH₃)CH₂-(4-Cl—C₆H₄) NH Ia1.1155 OCH₃ (CH₂)₃CH₃ CH(CH₃)CH₂-(4-Cl—C₆H₄) NH Ia1.1156 OCH₃ H CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) NH Ia1.1157 OCH₃ CH₃ CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) NH Ia1.1158 OCH₃ CH₂CH₃ CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) NH Ia1.1159 OCH₃ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) NH Ia1.1160 OCH₃ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) NH Ia1.1161 OCH₃ H (CH₂)₂-(2,4-Cl₂—C₆H₃) NH Ia1.1162 OCH₃ CH₃ (CH₂)₂-(2,4-Cl₂—C₆H₃) NH Ia1.1163 OCH₃ CH₂CH₃ (CH₂)₂-(2,4-Cl₂—C₆H₃) NH Ia1.1164 OCH₃ (CH₂)₂CH₃ (CH₂)₂-(2,4-Cl₂—C₆H₃) NH Ia1.1165 OCH₃ (CH₂)₃CH₃ (CH₂)₂-(2,4-Cl₂—C₆H₃) NH Ia1.1166 OCH₃ H CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) NH Ia1.1167 OCH₃ CH₃ CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) NH Ia1.1168 OCH₃ CH₂CH₃ CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) NH Ia1.1169 OCH₃ (CH₂)₂CH₃ CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) NH Ia1.1170 OCH₃ (CH₂)₃CH₃ CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) NH Ia1.1171 OCH₃ H CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) NH Ia1.1172 OCH₃ CH₃ CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) NH Ia1.1173 OCH₃ CH₂CH₃ CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) NH Ia1.1174 OCH₃ (CH₂)₂CH₃ CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) NH Ia1.1175 OCH₃ (CH₂)₃CH₃ CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) NH Ia1.1176 OCH₃ H CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) NH Ia1.1177 OCH₃ CH₃ CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) NH Ia1.1178 OCH₃ CH₂CH₃ CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) NH Ia1.1179 OCH₃ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) NH Ia1.1180 OCH₃ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) NH Ia1.1181 OCH₃ H (CH₂)₂—O—C₆H₅ NH Ia1.1182 OCH₃ CH₃ (CH₂)₂—O—C₆H₅ NH Ia1.1183 OCH₃ CH₂CH₃ (CH₂)₂—O—C₆H₅ NH Ia1.1184 OCH₃ (CH₂)₂CH₃ (CH₂)₂—O—C₆H₅ NH Ia1.1185 OCH₃ (CH₂)₃CH₃ (CH₂)₂—O—C₆H₅ NH Ia1.1186 OCH₃ H CH₂CH(CH₃)—O—C₆H₅ NH Ia1.1187 OCH₃ CH₃ CH₂CH(CH₃)—O—C₆H₅ NH Ia1.1188 OCH₃ CH₂CH₃ CH₂CH(CH₃)—O—C₆H₅ NH Ia1.1189 OCH₃ (CH₂)₂CH₃ CH₂CH(CH₃)—O—C₆H₅ NH Ia1.1190 OCH₃ (CH₂)₃CH₃ CH₂CH(CH₃)—O—C₆H₅ NH Ia1.1191 OCH₃ H CH(CH₃)CH₂—O—C₆H₅ NH Ia1.1192 OCH₃ CH₃ CH(CH₃)CH₂—O—C₆H₅ NH Ia1.1193 OCH₃ CH₂CH₃ CH(CH₃)CH₂—O—C₆H₅ NH Ia1.1194 OCH₃ (CH₂)₂CH₃ CH(CH₃)CH₂—O—C₆H₅ NH Ia1.1195 OCH₃ (CH₂)₃CH₃ CH(CH₃)CH₂—O—C₆H₅ NH Ia1.1196 OCH₃ H CH(CH₃)CH(CH₃)—O—C₆H₅ NH Ia1.1197 OCH₃ CH₃ CH(CH₃)CH(CH₃)—O—C₆H₅ NH Ia1.1198 OCH₃ CH₂CH₃ CH(CH₃)CH(CH₃)—O—C₆H₅ NH Ia1.1199 OCH₃ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)—O—C₆H₅ NH Ia1.1200 OCH₃ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)—O—C₆H₅ NH Ia1.1201 OCH₃ H (CH₂)₂—O-(4-Cl—C₆H₄) NH Ia1.1202 OCH₃ CH₃ (CH₂)₂—O-(4-Cl—C₆H₄) NH Ia1.1203 OCH₃ CH₂CH₃ (CH₂)₂—O-(4-Cl—C₆H₄) NH Ia1.1204 OCH₃ (CH₂)₂CH₃ (CH₂)₂—O-(4-Cl—C₆H₄) NH Ia1.1205 OCH₃ (CH₂)₃CH₃ (CH₂)₂—O-(4-Cl—C₆H₄) NH Ia1.1206 OCH₃ H CH₂CH(CH₃)—O-(4-Cl—C₆H₄) NH Ia1.1207 OCH₃ CH₃ CH₂CH(CH₃)—O-(4-Cl—C₆H₄) NH Ia1.1208 OCH₃ CH₂CH₃ CH₂CH(CH₃)—O-(4-Cl—C₆H₄) NH Ia1.1209 OCH₃ (CH₂)₂CH₃ CH₂CH(CH₃)—O-(4-Cl—C₆H₄) NH Ia1.1210 OCH₃ (CH₂)₃CH₃ CH₂CH(CH₃)—O-(4-Cl—C₆H₄) NH Ia1.1211 OCH₃ H CH(CH₃)CH₂—O-(4-Cl—C₆H₄) NH Ia1.1212 OCH₃ CH₃ CH(CH₃)CH₂—O-(4-Cl—C₆H₄) NH Ia1.1213 OCH₃ CH₂CH₃ CH(CH₃)CH₂—O-(4-Cl—C₆H₄) NH Ia1.1214 OCH₃ (CH₂)₂CH₃ CH(CH₃)CH₂—O-(4-Cl—C₆H₄) NH Ia1.1215 OCH₃ (CH₂)₃CH₃ CH(CH₃)CH₂—O-(4-Cl—C₆H₄) NH Ia1.1216 OCH₃ H CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) NH Ia1.1217 OCH₃ CH₃ CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) NH Ia1.1218 OCH₃ CH₂CH₃ CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) NH Ia1.1219 OCH₃ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) NH Ia1.1220 OCH₃ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) NH Ia1.1221 OCH₃ H (CH₂)₂—O-(2,4-Cl₂—C₆H₃) NH Ia1.1222 OCH₃ CH₃ (CH₂)₂—O-(2,4-Cl₂—C₆H₃) NH Ia1.1223 OCH₃ CH₂CH₃ (CH₂)₂—O-(2,4-Cl₂—C₆H₃) NH Ia1.1224 OCH₃ (CH₂)₂CH₃ (CH₂)₂—O-(2,4-Cl₂—C₆H₃) NH Ia1.1225 OCH₃ (CH₂)₃CH₃ (CH₂)₂—O-(2,4-Cl₂—C₆H₃) NH Ia1.1226 OCH₃ H CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NH Ia1.1227 OCH₃ CH₃ CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NH Ia1.1228 OCH₃ CH₂CH₃ CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NH Ia1.1229 OCH₃ (CH₂)₂CH₃ CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NH Ia1.1230 OCH₃ (CH₂)₃CH₃ CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NH Ia1.1231 OCH₃ H CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) NH Ia1.1232 OCH₃ CH₃ CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) NH Ia1.1233 OCH₃ CH₂CH₃ CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) NH Ia1.1234 OCH₃ (CH₂)₂CH₃ CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) NH Ia1.1235 CCH₃ (CH₂)₃CH₃ CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) NH Ia1.1236 OCH₃ H CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NH Ia1.1237 OCH₃ CH₃ CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NH Ia1.1238 OCH₃ CH₂CH₃ CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NH Ia1.1239 OCH₃ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NH Ia1.1240 OCH₃ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NH Ia1.1241 OCH₃ H CH₃ NCH₃ Ia1.1242 OCH₃ CH₃ CH₃ NCH₃ Ia1.1243 OCH₃ CH₂CH₃ CH₃ NCH₃ Ia1.1244 OCH₃ (CH₂)₂CH₃ CH₃ NCH₃ Ia1.1245 OCH₃ (CH₂)₃CH₃ CH₃ NCH₃ Ia1.1246 OCH₃ H C₂H₅ NCH₃ Ia1.1247 OCH₃ CH₃ C₂H₅ NCH₃ Ia1.1248 OCH₃ CH₂CH₃ C₂H₅ NCH₃ Ia1.1249 OCH₃ (CH₂)₂CH₃ C₂H₅ NCH₃ Ia1.1250 OCH₃ (CH₂)₃CH₃ C₂H₅ NCH₃ Ia1.1251 OCH₃ H (CH₂)₂CH₃ NCH₃ Ia1.1252 OCH₃ CH₃ (CH₂)₂CH₃ NCH₃ Ia1.1253 OCH₃ CH₂CH₃ (CH₂)₂CH₃ NCH₃ Ia1.1254 OCH₃ (CH₂)₂CH₃ (CH₂)₂CH₃ NCH₃ Ia1.1255 OCH₃ (CH₂)₃CH₃ (CH₂)₂CH₃ NCH₃ Ia1.1256 OCH₃ H CH(CH₃)₂ NCH₃ Ia1.1257 OCH₃ CH₃ CH(CH₃)₂ NCH₃ Ia1.1258 OCH₃ CH₂CH₃ CH(CH₃)₂ NCH₃ Ia1.1259 OCH₃ (CH₂)₂CH₃ CH(CH₃)₂ NCH₃ Ia1.1260 OCH₃ (CH₂)₃CH₃ CH(CH₃)₂ NCH₃ Ia1.1261 OCH₃ H (CH₂)₃CH₃ NCH₃ Ia1.1262 OCH₃ CH₃ (CH₂)₃CH₃ NCH₃ Ia1.1263 OCH₃ CH₂CH₃ (CH₂)₃CH₃ NCH₃ Ia1.1264 OCH₃ (CH₂)₂CH₃ (CH₂)₃CH₃ NCH₃ Ia1.1265 OCH₃ (CH₂)₃CH₃ (CH₂)₃CH₃ NCH₃ Ia1.1266 OCH₃ H CH₂CH(CH₃)₂ NCH₃ Ia1.1267 OCH₃ CH₃ CH₂CH(CH₃)₂ NCH₃ Ia1.1268 OCH₃ CH₂CH₃ CH₂CH(CH₃)₂ NCH₃ Ia1.1269 OCH₃ (CH₂)₂CH₃ CH₂CH(CH₃)₂ NCH₃ Ia1.1270 OCH₃ (CH₂)₃CH₃ CH₂CH(CH₃)₂ NCH₃ Ia1.1271 OCH₃ H CH(CH₃)CH₂CH₃ NCH₃ Ia1.1272 OCH₃ CH₃ CH(CH₃)CH₂CH₃ NCH₃ Ia1.1273 OCH₃ CH₂CH₃ CH(CH₃)CH₂CH₃ NCH₃ Ia1.1274 OCH₃ (CH₂)₂CH₃ CH(CH₃)CH₂CH₃ NCH₃ Ia1.1275 OCH₃ (CH₂)₃CH₃ CH(CH₃)CH₂CH₃ NCH₃ Ia1.1276 OCH₃ H (CH₂)₂—C₆H₅ NCH₃ Ia1.1277 OCH₃ CH₃ (CH₂)₂—C₆H₅ NCH₃ Ia1.1278 OCH₃ CH₂CH₃ (CH₂)₂—C₆H₅ NCH₃ Ia1.1279 OCH₃ (CH₂)₂CH₃ (CH₂)₂—C₆H₅ NCH₃ Ia1.1280 OCH₃ (CH₂)₃CH₃ (CH₂)₂—C₆H₅ NCH₃ Ia1.1281 OCH₃ H CH₂CH(CH₃)—C₆H₅ NCH₃ Ia1.1282 OCH₃ CH₃ CH₂CH(CH₃)—C₆H₅ NCH₃ Ia1.1283 OCH₃ CH₂CH₃ CH₂CH(CH₃)—C₆H₅ NCH₃ Ia1.1284 OCH₃ (CH₂)₂CH₃ CH₂CH(CH₃)—C₆H₅ NCH₃ Ia1.1285 OCH₃ (CH₂)₃CH₃ CH₂CH(CH₃)—C₆H₅ NCH₃ Ia1.1286 OCH₃ H CH(CH₃)CH₂—C₆H₅ NCH₃ Ia1.1287 OCH₃ CH₃ CH(CH₃)CH₂—C₆H₅ NCH₃ Ia1.1288 OCH₃ CH₂CH₃ CH(CH₃)CH₂—C₆H₅ NCH₃ Ia1.1289 OCH₃ (CH₂)₂CH₃ CH(CH₃)CH₂—C₆H₅ NCH₃ Ia1.1290 OCH₃ (CH₂)₃CH₃ CH(CH₃)CH₂—C₆H₅ NCH₃ Ia1.1291 OCH₃ H CH(CH₃)CH(CH₃)—C₆H₅ NCH₃ Ia1.1292 OCH₃ CH₃ CH(CH₃)CH(CH₃)—C₆H₅ NCH₃ Ia1.1293 OCH₃ CH₂CH₃ CH(CH₃)CH(CH₃)—C₆H₅ NCH₃ Ia1.1294 OCH₃ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)—C₆H₅ NCH₃ Ia1.1295 OCH₃ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)—C₆H₅ NCH₃ Ia1.1296 OCH₃ H (CH₂)₂-(4-Cl—C₆H₄) NCH₃ Ia1.1297 OCH₃ CH₃ (CH₂)₂-(4-Cl—C₆H₄) NCH₃ Ia1.1298 OCH₃ CH₂CH₃ (CH₂)₂-(4-Cl—C₆H₄) NCH₃ Ia1.1299 OCH₃ (CH₂)₂CH₃ (CH₂)₂-(4-Cl—C₆H₄) NCH₃ Ia1.1300 OCH₃ (CH₂)₃CH₃ (CH₂)₂-(4-Cl—C₆H₄) NCH₃ Ia1.1301 OCH₃ H CH₂CH(CH₃)-(4-Cl—C₆H₄) NCH₃ Ia1.1302 OCH₃ CH₃ CH₂CH(CH₃)-(4-Cl—C₆H₄) NCH₃ Ia1.1303 OCH₃ CH₂CH₃ CH₂CH(CH₃)-(4-Cl—C₆H₄) NCH₃ Ia1.1304 OCH₃ (CH₂)₂CH₃ CH₂CH(CH₃)-(4-Cl—C₆H₄) NCH₃ Ia1.1305 OCH₃ (CH₂)₃CH₃ CH₂CH(CH₃)-(4-Cl—C₆H₄) NCH₃ Ia1.1306 OCH₃ H CH(CH₃)CH₂-(4-Cl—C₆H₄) NCH₃ Ia1.1307 OCH₃ CH₃ CH(CH₃)CH₂-(4-Cl—C₆H₄) NCH₃ Ia1.1308 OCH₃ CH₂CH₃ CH(CH₃)—CH₂-(4-Cl—C₆H₄) NCH₃ Ia1.1309 OCH₃ (CH₂)₂CH₃ CH(CH₃)CH₂-(4-Cl—C₆H₄) NCH₃ Ia1.1310 OCH₃ (CH₂)₃CH₃ CH(CH₃)CH₂-(4-Cl—C₆H₄) NCH₃ Ia1.1311 OCH₃ H CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) NCH₃ Ia1.1312 OCH₃ CH₃ CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) NCH₃ Ia1.1313 OCH₃ CH₂CH₃ CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) NCH₃ Ia1.1314 OCH₃ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) NCH₃ Ia1.1315 OCH₃ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) NCH₃ Ia1.1316 OCH₃ H (CH₂)₂-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1317 OCH₃ CH₃ (CH₂)₂-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1318 OCH₃ CH₂CH₃ (CH₂)₂-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1319 OCH₃ (CH₂)₂CH₃ (CH₂)₂-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1320 OCH₃ (CH₂)₃CH₃ (CH₂)₂-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1321 OCH₃ H CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1322 OCH₃ CH₃ CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1323 OCH₃ CH₂CH₃ CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1324 OCH₃ (CH₂)₂CH₃ CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1325 OCH₃ (CH₂)₃CH₃ CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1326 OCH₃ H CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1327 OCH₃ CH₃ CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1328 OCH₃ CH₂CH₃ CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1329 OCH₃ (CH₂)₂CH₃ CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1330 OCH₃ (CH₂)₃CH₃ CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1331 OCH₃ H CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1332 OCH₃ CH₃ CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1333 OCH₃ CH₂CH₃ CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1334 OCH₃ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1335 OCH₃ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1336 OCH₃ H (CH₂)₂—O—C₆H₅ NCH₃ Ia1.1337 OCH₃ CH₃ (CH₂)₂—O—C₆H₅ NCH₃ Ia1.1338 OCH₃ CH₂CH₃ (CH₂)₂—O—C₆H₅ NCH₃ Ia1.1339 OCH₃ (CH₂)₂CH₃ (CH₂)₂—O—C₆H₅ NCH₃ Ia1.1340 OCH₃ (CH₂)₃CH₃ (CH₂)₂—O—C₆H₅ NCH₃ Ia1.1341 OCH₃ H CH₂CH(CH₃)—O—C₆H₅ NCH₃ Ia1.1342 OCH₃ CH₃ CH₂CH(CH₃)—O—C₆H₅ NCH₃ Ia1.1343 OCH₃ CH₂CH₃ CH₂CH(CH₃)—O—C₆H₅ NCH₃ Ia1.1344 OCH₃ (CH₂)₂CH₃ CH₂CH(CH₃)—O—C₆H₅ NCH₃ Ia1.1345 OCH₃ (CH₂)₃CH₃ CH₂CH(CH₃)—O—C₆H₅ NCH₃ Ia1.1346 OCH₃ H CH(CH₃)CH₂—O—C₆H₅ NCH₃ Ia1.1347 OCH₃ CH₃ CH(CH₃)CH₂—O—C₆H₅ NCH₃ Ia1.1348 OCH₃ CH₂CH₃ CH(CH₃)CH₂—O—C₆H₅ NCH₃ Ia1.1349 OCH₃ (CH₂)₂CH₃ CH(CH₃)CH₂—O—C₆H₅ NCH₃ Ia1.1350 OCH₃ (CH₂)₃CH₃ CH(CH₃)CH₂—O—C₆H₅ NCH₃ Ia1.1351 OCH₃ H CH(CH₃)CH(CH₃)—O—C₆H₅ NCH₃ Ia1.1352 OCH₃ CH₃ CH(CH₃)CH(CH₃)—O—C₆H₅ NCH₃ Ia1.1353 OCH₃ CH₂CH₃ CH(CH₃)CH(CH₃)—O—C₆H₅ NCH₃ Ia1.1354 OCH₃ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)—O—C₆H₅ NCH₃ Ia1.1355 OCH₃ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)—O—C₆H₅ NCH₃ Ia1.1356 OCH₃ H (CH₂)₂—O-(4-Cl—C₆H₄) NCH₃ Ia1.1357 OCH₃ CH₃ (CH₂)₂—O-(4-Cl—C₆H₄) NCH₃ Ia1.1358 OCH₃ CH₂CH₃ (CH₂)₂—O-(4-Cl—C₆H₄) NCH₃ Ia1.1359 OCH₃ (CH₂)₂CH₃ (CH₂)₂—O-(4-Cl—C₆H₄) NCH₃ Ia1.1360 OCH₃ (CH₂)₃CH₃ (CH₂)₂—O-(4-Cl—C₆H₄) NCH₃ Ia1.1361 OCH₃ H CH₂CH(CH₃)—O-(4-Cl—C₆H₄) NCH₃ Ia1.1362 OCH₃ CH₃ CH₂CH(CH₃)—O-(4-Cl—C₆H₄) NCH₃ Ia1.1363 OCH₃ CH₂CH₃ CH₂CH(CH₃)—O-(4-Cl—C₆H₄) NCH₃ Ia1.1364 OCH₃ (CH₂)₂CH₃ CH₂CH(CH₃)—O-( 4-Cl—C₆H₄) NCH₃ Ia1.1365 OCH₃ (CH₂)₃CH₃ CH₂CH(CH₃)—O-(4-Cl—C₆H₄) NCH₃ Ia1.1366 OCH₃ H CH(CH₃)CH₂—O-(4-Cl—C₆H₄) NCH₃ Ia1.1367 OCH₃ CH₃ CH(CH₃)CH₂—O-(4-Cl—C₆H₄) NCH₃ Ia1.1368 OCH₃ CH₂CH₃ CH(CH₃)CH₂—O-(4-Cl—C₆H₄) NCH₃ Ia1.1369 OCH₃ (CH₂)₂CH₃ CH(CH₃)CH₂—O-(4-Cl—C₆H₄) NCH₃ Ia1.1370 OCH₃ (CH₂)₃CH₃ CH(CH₃)CH₂—O-(4-Cl—C₆H₄) NCH₃ Ia1.1371 OCH₃ H CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) NCH₃ Ia1.1372 OCH₃ CH₃ CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) NCH₃ Ia1.1373 OCH₃ CH₂CH₃ CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) NCH₃ Ia1.1374 OCH₃ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) NCH₃ Ia1.1375 OCH₃ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) NCH₃ Ia1.1376 OCH₃ H (CH₂)₂—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1377 OCH₃ CH₃ (CH₂)₂—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1378 OCH₃ CH₂CH₃ (CH₂)₂—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1379 OCH₃ (CH₂)₂CH₃ (CH₂)₂—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1380 OCH₃ (CH₂)₃CH₃ (CH₂)₂—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1381 OCH₃ H CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1382 OCH₃ CH₃ CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1383 OCH₃ CH₂CH₃ CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1384 OCH₃ (CH₂)₂CH₃ CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1385 OCH₃ (CH₂)₃CH₃ CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1386 OCH₃ H CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1387 OCH₃ CH₃ CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1388 OCH₃ CH₂CH₃ CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1389 OCH₃ (CH₂)₂CH₃ CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1390 OCH₃ (CH₂)₃CH₃ CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1391 OCH₃ H CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1392 OCH₃ CH₃ CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1393 OCH₃ CH₂CH₃ CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1394 OCH₃ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1395 OCH₃ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1396 CF₃ H CH₃ O Ia1.1397 CF₃ CH₃ CH₃ O Ia1.1398 CF₃ CH₂CH₃ CH₃ O Ia1.1399 CF₃ (CH₂)₂CH₃ CH₃ O Ia1.1400 CF₃ (CH₂)₃CH₃ CH₃ O Ia1.1401 CF₃ H C₂H₅ O Ia1.1402 CF₃ CH₃ C₂H₅ O Ia1.1403 CF₃ CH₂CH₃ C₂H₅ O Ia1.1404 CF₃ (CH₂)₂CH₃ C₂H₅ O Ia1.1405 CF₃ (CH₂)₃CH₃ C₂H₅ O Ia1.1406 CF₃ H (CH₂)₂CH₃ O Ia1.1407 CF₃ CH₃ (CH₂)₂CH₃ O Ia1.1408 CF₃ CH₂CH₃ (CH₂)₂CH₃ O Ia1.1409 CF₃ (CH₂)₂CH₃ (CH₂)₂CH₃ O Ia1.1410 CF₃ (CH₂)₃CH₃ (CH₂)₂CH₃ O Ia1.1411 CF₃ H CH(CH₃)₂ O Ia1.1412 CF₃ CH₃ CH(CH₃)₂ O Ia1.1413 CF₃ CH₂CH₃ CH(CH₃)₂ O Ia1.1414 CF₃ (CH₂)₂CH₃ CH(CH₃)₂ O Ia1.1415 CF₃ (CH₂)₃CH₃ CH(CH₃)₂ O Ia1.1416 CF₃ H (CH₂)₃CH₃ O Ia1.1417 CF₃ CH₃ (CH₂)₃CH₃ O Ia1.1418 CF₃ CH₂CH₃ (CH₂)₃CH₃ O Ia1.1419 CF₃ (CH₂)₂CH₃ (CH₂)₃CH₃ O Ia1.1420 CF₃ (CH₂)₃CH₃ (CH₂)₃CH₃ O Ia1.1421 CF₃ H CH₂CH(CH₃)₂ O Ia1.1422 CF₃ CH₃ CH₂CH(CH₃)₂ O Ia1.1423 CF₃ CH₂CH₃ CH₂CH(CH₃)₂ O Ia1.1424 CF₃ (CH₂)₂CH₃ CH₂CH(CH₃)₂ O Ia1.1425 CF₃ (CH₂)₃CH₃ CH₂CH(CH₃)₂ O Ia1.1426 CF₃ H CH(CH₃)CH₂CH₃ O Ia1.1427 CF₃ CH₃ CH(CH₃)CH₂CH₃ O Ia1.1428 CF₃ CH₂CH₃ CH(CH₃)CH₂CH₃ O Ia1.1429 CF₃ (CH₂)₂CH₃ CH(CH₃)CH₂CH₃ O Ia1.1430 CF₃ (CH₂)₃CH₃ CH(CH₃)CH₂CH₃ O Ia1.1431 CF₃ H (CH₂)₂—C₆H₅ O Ia1.1432 CF₃ CH₃ (CH₂)₂—C₆H₅ O Ia1.1433 CF₃ CH₂CH₃ (CH₂)₂—C₆H₅ O Ia1.1434 CF₃ (CH₂)₂CH₃ (CH₂)₂—C₆H₅ O Ia1.1435 CF₃ (CH₂)₃CH₃ (CH₂)₂—C₆H₅ O Ia1.1436 CF₃ H CH₂CH(CH₃)—C₆H₅ O Ia1.1437 CF₃ CH₃ CH₂CH(CH₃)—C₆H₅ O Ia1.1438 CF₃ CH₂CH₃ CH₂CH(CH₃)—C₆H₅ O Ia1.1439 CF₃ (CH₂)₂CH₃ CH₂CH(CH₃)—C₆H₅ O Ia1.1440 CF₃ (CH₂)₃CH₃ CH₂CH(CH₃)—C₆H₅ O Ia1.1441 CF₃ H CH(CH₃)CH₂—C₆H₅ O Ia1.1442 CF₃ CH₃ CH(CH₃)CH₂—C₆H₅ O Ia1.1443 CF₃ CH₂CH₃ CH(CH₃)CH₂—C₆H₅ O Ia1.1444 CF₃ (CH₂)₂CH₃ CH(CH₃)CH₂—C₆H₅ O Ia1.1445 CF₃ (CH₂)₃CH₃ CH(CH₃)CH₂—C₆H₅ O Ia1.1446 CF₃ H CH(CH₃)CH(CH₃)—C₆H₅ O Ia1.1447 CF₃ CH₃ CH(CH₃)CH(CH₃)—C₆H₅ O Ia1.1448 CF₃ CH₂CH₃ CH(CH₃)CH(CH₃)—C₆H₅ O Ia1.1449 CF₃ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)—C₆H₅ O Ia1.1450 CF₃ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)—C₆H₅ O Ia1.1451 CF₃ H (CH₂)₂-(4-Cl—C₆H₄) O Ia1.1452 CF₃ CH₃ (CH₂)₂-(4-Cl—C₆H₄) O Ia1.1453 CF₃ CH₂CH₃ (CH₂)₂-(4-Cl—C₆H₄) O Ia1.1454 CF₃ (CH₂)₂CH₃ (CH₂)₂-(4-Cl—C₆H₄) O Ia1.1455 CF₃ (CH₂)₃CH₃ (CH₂)₂-(4-Cl—C₆H₄) O Ia1.1456 CF₃ H CH₂CH(CH₃)-(4-Cl—C₆H₄) O Ia1.1457 CF₃ CH₃ CH₂CH(CH₃)-(4-Cl—C₆H₄) O Ia1.1458 CF₃ CH₂CH₃ CH₂CH(CH₃)-(4-Cl—C₆H₄) O Ia1.1459 CF₃ (CH₂)₂CH₃ CH₂CH(CH₃)-(4-Cl—C₆H₄) O Ia1.1460 CF₃ (CH₂)₃CH₃ CH₂CH(CH₃)-(4-Cl—C₆H₄) O Ia1.1461 CF₃ H CH(CH₃)CH₂-(4-Cl—C₆H₄) O Ia1.1462 CF₃ CH₃ CH(CH₃)CH₂-(4-Cl—C₆H₄) O Ia1.1463 CF₃ CH₂CH₃ CH(CH₃)CH₂-(4-Cl—C₆H₄) O Ia1.1464 CF₃ (CH₂)₂CH₃ CH(CH₃)CH₂-(4-Cl—C₆H₄) O Ia1.1465 CF₃ (CH₂)₃CH₃ CH(CH₃)CH₂-(4-Cl—C₆H₄) O Ia1.1466 CF₃ H CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) O Ia1.1467 CF₃ CH₃ CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) O Ia1.1468 CF₃ CH₂CH₃ CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) O Ia1.1469 CF₃ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) O Ia1.1470 CF₃ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) O Ia1.1471 CF₃ H (CH₂)₂-(2,4-Cl₂—C₆H₃) O Ia1.1472 CF₃ CH₃ (CH₂)₂-(2,4-Cl₂—C₆H₃) O Ia1.1473 CF₃ CH₂CH₃ (CH₂)₂-(2,4-Cl₂—C₆H₃) O Ia1.1474 CF₃ (CH₂)₂CH₃ (CH₂)₂-(2,4-Cl₂—C₆H₃) O Ia1.1475 CF₃ (CH₂)₃CH₃ (CH₂)₂-(2,4-Cl₂—C₆H₃) O Ia1.1476 CF₃ H CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) O Ia1.1477 CF₃ CH₃ CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) O Ia1.1478 CF₃ CH₂CH₃ CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) O Ia1.1479 CF₃ (CH₂)₂CH₃ CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) O Ia1.1480 CF₃ (CH₂)₃CH₃ CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) O Ia1.1481 CF₃ H CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) O Ia1.1482 CF₃ CH₃ CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) O Ia1.1483 CF₃ CH₂CH₃ CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) O Ia1.1484 CF₃ (CH₂)₂CH₃ CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) O Ia1.1485 CF₃ (CH₂)₃CH₃ CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) O Ia1.1486 CF₃ H CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) O Ia1.1487 CF₃ CH₃ CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) O Ia1.1488 CF₃ CH₂CH₃ CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) O Ia1.1489 CF₃ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) O Ia1.1490 CF₃ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) O Ia1.1491 CF₃ H (CH₂)₂—O—C₆H₅ O Ia1.1492 CF₃ CH₃ (CH₂)₂—O—C₆H₅ O Ia1.1493 CF₃ CH₂CH₃ (CH₂)₂—O—C₆H₅ O Ia1.1494 CF₃ (CH₂)₂CH₃ (CH₂)₂—O—C₆H₅ O Ia1.1495 CF₃ (CH₂)₃CH₃ (CH₂)₂—O—C₆H₅ O Ia1.1496 CF₃ H CH₂CH(CH₃)—O—C₆H₅ O Ia1.1497 CF₃ CH₃ CH₂CH(CH₃)—O—C₆H₅ O Ia1.1498 CF₃ CH₂CH₃ CH₂CH(CH₃)—O—C₆H₅ O Ia1.1499 CF₃ (CH₂)₂CH₃ CH₂CH(CH₃)—O—C₆H₅ O Ia1.1500 CF₃ (CH₂)₃CH₃ CH₂CH(CH₃)—O—C₆H₅ O Ia1.1501 CF₃ H CH(CH₃)CH₂—O—C₆H₅ O Ia1.1502 CF₃ CH₃ CH(CH₃)CH₂—O—C₆H₅ O Ia1.1503 CF₃ CH₂CH₃ CH(CH₃)CH₂—O—C₆H₅ O Ia1.1504 CF₃ (CH₂)₂CH₃ CH(CH₃)CH₂—O—C₆H₅ O Ia1.1505 CF₃ (CH₂)₃CH₃ CH(CH₃)CH₂—O—C₆H₅ O Ia1.1506 CF₃ H CH(CH₃)CH(CH₃)—O—C₆H₅ O Ia1.1507 CF₃ CH₃ CH(CH₃)CH(CH₃)—O—C₆H₅ O Ia1.1508 CF₃ CH₂CH₃ CH(CH₃)CH(CH₃)—O—C₆H₅ O Ia1.1509 CF₃ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)—O—C₆H₅ O Ia1.1510 CF₃ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)—O—C₆H₅ O Ia1.1511 CF₃ H (CH₂)₂—O-(4-Cl—C₆H₄) O Ia1.1512 CF₃ CH₃ (CH₂)₂—O-(4-Cl—C₆H₄) O Ia1.1513 CF₃ CH₂CH₃ (CH₂)₂—O-(4-Cl—C₆H₄) O Ia1.1514 CF₃ (CH₂)₂CH₃ (CH₂)₂—O-(4-Cl—C₆H₄) O Ia1.1515 CF₃ (CH₂)₃CH₃ (CH₂)₂—O-(4-Cl—C₆H₄) O Ia1.1516 CF₃ H CH₂CH(CH₃)—O-(4-Cl—C₆H₄) O Ia1.1517 CF₃ CH₃ CH₂CH(CH₃)—O-(4-Cl—C₆H₄) O Ia1.1518 CF₃ CH₂CH₃ CH₂CH(CH₃)—O-(4-Cl—C₆H₄) O Ia1.1519 CF₃ (CH₂)₂CH₃ CH₂CH(CH₃)—O-(4-Cl—C₆H₄) O Ia1.1520 CF₃ (CH₂)₃CH₃ CH₂CH(CH₃)—O-(4-Cl—C₆H₄) O Ia1.1521 CF₃ H CH(CH₃)CH₂—O-(4-Cl—C₆H₄) O Ia1.1522 CF₃ CH₃ CH(CH₃)CH₂—O-(4-Cl—C₆H₄) O Ia1.1523 CF₃ CH₂CH₃ CH(CH₃)CH₂—O-(4-Cl—C₆H₄) O Ia1.1524 CF₃ (CH₂)₂CH₃ CH(CH₃)CH₂—O-(4-Cl—C₆H₄) O Ia1.1525 CF₃ (CH₂)₃CH₃ CH(CH₃)CH₂—O-(4-Cl—C₆H₄) O Ia1.1526 CF₃ H CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) O Ia1.1527 CF₃ CH₃ CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) O Ia1.1528 CF₃ CH₂CH₃ CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) O Ia1.1529 CF₃ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) O Ia1.1530 CF₃ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) O Ia1.1531 CF₃ H (CH₂)₂—O-(2,4-Cl₂—C₆H₃) O Ia1.1532 CF₃ CH₃ (CH₂)₂—O-(2,4-Cl₂—C₆H₃) O Ia1.1533 CF₃ CH₂CH₃ (CH₂)₂—O-(2,4-Cl₂—C₆H₃) O Ia1.1534 CF₃ (CH₂)₂CH₃ (CH₂)₂—O-(2,4-Cl₂—C₆H₃) O Ia1.1535 CF₃ (CH₂)₃CH₃ (CH₂)₂—O-(2,4-Cl₂—C₆H₃) O Ia1.1536 CF₃ H CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) O Ia1.1537 CF₃ CH₃ CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) O Ia1.1538 CF₃ CH₂CH₃ CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) O Ia1.1539 CF₃ (CH₂)₂CH₃ CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) O Ia1.1540 CF₃ (CH₂)₃CH₃ CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) O Ia1.1541 CF₃ H CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) O Ia1.1542 CF₃ CH₃ CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) O Ia1.1543 CF₃ CH₂CH₃ CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) O Ia1.1544 CF₃ (CH₂)₂CH₃ CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) O Ia1.1545 CF₃ (CH₂)₃CH₃ CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) O Ia1.1546 CF₃ H CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) O Ia1.1547 CF₃ CH₃ CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) O Ia1.1548 CF₃ CH₂CH₃ CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) O Ia1.1549 CF₃ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) O Ia1.1550 CF₃ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) O Ia1.1551 CF₃ H CH₃ NH Ia1.1552 CF₃ CH₃ CH₃ NH Ia1.1553 CF₃ CH₂CH₃ CH₃ NH Ia1.1554 CF₃ (CH₂)₂CH₃ CH₃ NH Ia1.1555 CF₃ (CH₂)₃CH₃ CH₃ NH Ia1.1556 CF₃ H C₂H₅ NH Ia1.1557 CF₃ CH₃ C₂H₅ NH Ia1.1558 CF₃ CH₂CH₃ C₂H₅ NH Ia1.1559 CF₃ (CH₂)₂CH₃ C₂H₅ NH Ia1.1560 CF₃ (CH₂)₃CH₃ C₂H₅ NH Ia1.1561 CF₃ H (CH₂)₂CH₃ NH Ia1.1562 CF₃ CH₃ (CH₂)₂CH₃ NH Ia1.1563 CF₃ CH₂CH₃ (CH₂)₂CH₃ NH Ia1.1564 CF₃ (CH₂)₂CH₃ (CH₂)₂CH₃ NH Ia1.1565 CF₃ (CH₂)₃CH₃ (CH₂)₂CH₃ NH Ia1.1566 CF₃ H CH(CH₃)₂ NH Ia1.1567 CF₃ CH₃ CH(CH₃)₂ NH Ia1.1568 CF₃ CH₂CH₃ CH(CH₃)₂ NH Ia1.1569 CF₃ (CH₂)₂CH₃ CH(CH₃)₂ NH Ia1.1570 CF₃ (CH₂)₃CH₃ CH(CH₃)₂ NH Ia1.1571 CF₃ H (CH₂)₃CH₃ NH Ia1.1572 CF₃ CH₃ (CH₂)₃CH₃ NH Ia1.1573 CF₃ CH₂CH₃ (CH₂)₃CH₃ NH Ia1.1574 CF₃ (CH₂)₂CH₃ (CH₂)₃CH₃ NH Ia1.1575 CF₃ (CH₂)₃CH₃ (CH₂)₃CH₃ NH Ia1.1576 CF₃ H CH₂CH(CH₃)₂ NH Ia1.1577 CF₃ CH₃ CH₂CH(CH₃)₂ NH Ia1.1578 CF₃ CH₂CH₃ CH₂CH(CH₃)₂ NH Ia1.1579 CF₃ (CH₂)₂CH₃ CH₂CH(CH₃)₂ NH Ia1.1580 CF₃ (CH₂)₃CH₃ CH₂CH(CH₃)₂ NH Ia1.1581 CF₃ H CH(CH₃)CH₂CH₃ NH Ia1.1582 CF₃ CH₃ CH(CH₃)CH₂CH₃ NH Ia1.1583 CF₃ CH₂CH₃ CH(CH₃)CH₂CH₃ NH Ia1.1584 CF₃ (CH₂)₂CH₃ CH(CH₃)CH₂CH₃ NH Ia1.1585 CF₃ (CH₂)₃CH₃ CH(CH₃)CH₂CH₃ NH Ia1.1586 CF₃ H (CH₂)₂—C₆H₅ NH Ia1.1587 CF₃ CH₃ (CH₂)₂—C₆H₅ NH Ia1.1588 CF₃ CH₂CH₃ (CH₂)₂—C₆H₅ NH Ia1.1589 CF₃ (CH₂)₂CH₃ (CH₂)₂—C₆H₅ NH Ia1.1590 CF₃ (CH₂)₃CH₃ (CH₂)₂—C₆H₅ NH Ia1.1591 CF₃ H CH₂CH(CH₃)—C₆H₅ NH Ia1.1592 CF₃ CH₃ CH₂CH(CH₃)—C₆H₅ NH Ia1.1593 CF₃ CH₂CH₃ CH₂CH(CH₃)—C₆H₅ NH Ia1.1594 CF₃ (CH₂)₂CH₃ CH₂CH(CH₃)—C₆H₅ NH Ia1.1595 CF₃ (CH₂)₃CH₃ CH₂CH(CH₃)—C₆H₅ NH Ia1.1596 CF₃ H CH(CH₃)CH₂—C₆H₅ NH Ia1.1597 CF₃ CH₃ CH(CH₃)CH₂—C₆H₅ NH Ia1.1598 CF₃ CH₂CH₃ CH(CH₃)CH₂—C₆H₅ NH Ia1.1599 CF₃ (CH₂)₂CH₃ CH(CH₃)CH₂—C₆H₅ NH Ia1.1600 CF₃ (CH₂)₃CH₃ CH(CH₃)CH₂—C₆H₅ NH Ia1.1601 CF₃ H CH(CH₃)CH(CH₃)—C₆H₅ NH Ia1.1602 CF₃ CH₃ CH(CH₃)CH(CH₃)—C₆H₅ NH Ia1.1603 CF₃ CH₂CH₃ CH(CH₃)CH(CH₃)—C₆H₅ NH Ia1.1604 CF₃ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)—C₆H₅ NH Ia1.1605 CF₃ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)—C₆H₅ NH Ia1.1606 CF₃ H (CH₂)₂-(4-Cl—C₆H₄) NH Ia1.1607 CF₃ CH₃ (CH₂)₂-(4-Cl—C₆H₄) NH Ia1.1608 CF₃ CH₂CH₃ (CH₂)₂-(4-Cl—C₆H₄) NH Ia1.1609 CF₃ (CH₂)₂CH₃ (CH₂)₂-(4-Cl—C₆H₄) NH Ia1.1610 CF₃ (CH₂)₃CH₃ (CH₂)₂-(4-Cl—C₆H₄) NH Ia1.1611 CF₃ H CH₂CH(CH₃)-(4-Cl—C₆H₄) NH Ia1.1612 CF₃ CH₃ CH₂CH(CH₃)-(4-Cl—C₆H₄) NH Ia1.1613 CF₃ CH₂CH₃ CH₂CH(CH₃)-(4-Cl—C₆H₄) NH Ia1.1614 CF₃ (CH₂)₂CH₃ CH₂CH(CH₃)-(4-Cl—C₆H₄) NH Ia1.1615 CF₃ (CH₂)₃CH₃ CH₂CH(CH₃)-(4-Cl—C₆H₄) NH Ia1.1616 CF₃ H CH(CH₃)CH₂-(4-Cl—C₆H₄) NH Ia1.1617 CF₃ CH₃ CH(CH₃)CH₂-(4-Cl—C₆H₄) NH Ia1.1618 CF₃ CH₂CH₃ CH(CH₃)CH₂-(4-Cl—C₆H₄) NH Ia1.1619 CF₃ (CH₂)₂CH₃ CH(CH₃)CH₂-(4-Cl—C₆H₄) NH Ia1.1620 CF₃ (CH₂)₃CH₃ CH(CH₃)CH₂-(4-Cl—C₆H₄) NH Ia1.1621 CF₃ H CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) NH Ia1.1622 CF₃ CH₃ CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) NH Ia1.1623 CF₃ CH₂CH₃ CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) NH Ia1.1624 CF₃ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) NH Ia1.1625 CF₃ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) NH Ia1.1626 CF₃ H (CH₂)₂-(2,4-Cl₂—C₆H₃) NH Ia1.1627 CF₃ CH₃ (CH₂)₂-(2,4-Cl₂—C₆H₃) NH Ia1.1628 CF₃ CH₂CH₃ (CH₂)₂-(2,4-Cl₂—C₆H₃) NH Ia1.1629 CF₃ (CH₂)₂CH₃ (CH₂)₂-(2,4-Cl₂—C₆H₃) NH Ia1.1630 CF₃ (CH₂)₃CH₃ (CH₂)₂-(2,4-Cl₂—C₆H₃) NH Ia1.1631 CF₃ H CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) NH Ia1.1632 CF₃ CH₃ CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) NH Ia1.1633 CF₃ CH₂CH₃ CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) NH Ia1.1634 CF₃ (CH₂)₂CH₃ CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) NH Ia1.1635 CF₃ (CH₂)₃CH₃ CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) NH Ia1.1636 CF₃ H CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) NH Ia1.1637 CF₃ CH₃ CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) NH Ia1.1638 CF₃ CH₂CH₃ CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) NH Ia1.1639 CF₃ (CH₂)₂CH₃ CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) NH Ia1.1640 CF₃ (CH₂)₃CH₃ CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) NH Ia1.1641 CF₃ H CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) NH Ia1.1642 CF₃ CH₃ CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) NH Ia1.1643 CF₃ CH₂CH₃ CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) NH Ia1.1644 CF₃ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) NH Ia1.1645 CF₃ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) NH Ia1.1646 CF₃ H (CH₂)₂—O—C₆H₅ NH Ia1.1647 CF₃ CH₃ (CH₂)₂—O—C₆H₅ NH Ia1.1648 CF₃ CH₂CH₃ (CH₂)₂—O—C₆H₅ NH Ia1.1649 CF₃ (CH₂)₂CH₃ (CH₂)₂—O—C₆H₅ NH Ia1.1650 CF₃ (CH₂)₃CH₃ (CH₂)₂—O—C₆H₅ NH Ia1.1651 CF₃ H CH₂CH(CH₃)—O—C₆H₅ NH Ia1.1652 CF₃ CH₃ CH₂CH(CH₃)—O—C₆H₅ NH Ia1.1653 CF₃ CH₂CH₃ CH₂CH(CH₃)—O—C₆H₅ NH Ia1.1654 CF₃ (CH₂)₂CH₃ CH₂CH(CH₃)—O—C₆H₅ NH Ia1.1655 CF₃ (CH₂)₃CH₃ CH₂CH(CH₃)—O—C₆H₅ NH Ia1.1656 CF₃ H CH(CH₃)CH₂—O—C₆H₅ NH Ia1.1657 CF₃ CH₃ CH(CH₃)CH₂—O—C₆H₅ NH Ia1.1658 CF₃ CH₂CH₃ CH(CH₃)CH₂—O—C₆H₅ NH Ia1.1659 CF₃ (CH₂)₂CH₃ CH(CH₃)CH₂—O—C₆H₅ NH Ia1.1660 CF₃ (CH₂)₃CH₃ CH(CH₃)CH₂—O—C₆H₅ NH Ia1.1661 CF₃ H CH(CH₃)CH(CH₃)—O—C₆H₅ NH Ia1.1662 CF₃ CH₃ CH(CH₃)CH(CH₃)—O—C₆H₅ NH Ia1.1663 CF₃ CH₂CH₃ CH(CH₃)CH(CH₃)—O—C₆H₅ NH Ia1.1664 CF₃ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)—O—C₆H₅ NH Ia1.1665 CF₃ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)—O—C₆H₅ NH Ia1.1666 CF₃ H (CH₂)₂—O-(4-Cl—C₆H₄) NH Ia1.1667 CF₃ CH₃ (CH₂)₂—O-(4-Cl—C₆H₄) NH Ia1.1668 CF₃ CH₂CH₃ (CH₂)₂—O-(4-Cl—C₆H₄) NH Ia1.1669 CF₃ (CH₂)₂CH₃ (CH₂)₂—O-(4-Cl—C₆H₄) NH Ia1.1670 CF₃ (CH₂)₃CH₃ (CH₂)₂—O-(4-Cl—C₆H₄) NH Ia1.1671 CF₃ H CH₂CH(CH₃)—O-(4-Cl—C₆H₄) NH Ia1.1672 CF₃ CH₃ CH₂CH(CH₃)—O-(4-Cl—C₆H₄) NH Ia1.1673 CF₃ CH₂CH₃ CH₂CH (CH₃)—O-(4-Cl—C₆H₄) NH Ia1.1674 CF₃ (CH₂)₂CH₃ CH₂CH(CH₃)—O-(4-Cl—C₆H₄) NH Ia1.1675 CF₃ (CH₂)₃CH₃ CH₂CH(CH₃)—O-(4-Cl—C₆H₄) NH Ia1.1676 CF₃ H CH(CH₃)CH₂—O-(4-Cl—C₆H₄) NH Ia1.1677 CF₃ CH₃ CH(CH₃)CH₂—O-(4-Cl—C₆H₄) NH Ia1.1678 CF₃ CH₂CH₃ CH(CH₃)CH₂—O-(4-Cl—C₆H₄) NH Ia1.1679 CF₃ (CH₂)₂CH₃ CH(CH₃)CH₂—O-(4-Cl—C₆H₄) NH Ia1.1680 CF₃ (CH₂)₃CH₃ CH(CH₃)CH₂—O-(4-Cl—C₆H₄) NH Ia1.1681 CF₃ H CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) NH Ia1.1682 CF₃ CH₃ CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) NH Ia1.1683 CF₃ CH₂CH₃ CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) NH Ia1.1684 CF₃ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) NH Ia1.1685 CF₃ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) NH Ia1.1686 CF₃ H (CH₂)₂—O-(2,4-Cl₂—C₆H₃) NH Ia1.1687 CF₃ CH₃ (CH₂)₂—O-(2,4-Cl₂—C₆H₃) NH Ia1.1688 CF₃ CH₂CH₃ (CH₂)₂—O-(2,4-Cl₂—C₆H₃) NH Ia1.1689 CF₃ (CH₂)₂CH₃ (CH₂)₂—O-(2,4-Cl₂—C₆H₃) NH Ia1.1690 CF₃ (CH₂)₃CH₃ (CH₂)₂—O-(2,4-Cl₂—C₆H₃) NH Ia1.1691 CF₃ H CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NH Ia1.1692 CF₃ CH₃ CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NH Ia1.1693 CF₃ CH₂CH₃ CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NH Ia1.1694 CF₃ (CH₂)₂CH₃ CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NH Ia1.1695 CF₃ (CH₂)₃CH₃ CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NH Ia1.1696 CF₃ H CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) NH Ia1.1697 CF₃ CH₃ CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) NH Ia1.1698 CF₃ CH₂CH₃ CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) NH Ia1.1699 CF₃ (CH₂)₂CH₃ CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) NH Ia1.1700 CF₃ (CH₂)₃CH₃ CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) NH Ia1.1701 CF₃ H CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NH Ia1.1702 CF₃ CH₃ CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NH Ia1.1703 CF₃ CH₂CH₃ CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NH Ia1.1704 CF₃ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NH Ia1.1705 CF₃ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NH Ia1.1706 CF₃ H CH₃ NCH₃ Ia1.1707 CF₃ CH₃ CH₃ NCH₃ Ia1.1708 CF₃ CH₂CH₃ CH₃ NCH₃ Ia1.1709 CF₃ (CH₂)₂CH₃ CH₃ NCH₃ Ia1.1710 CF₃ (CH₂)₃CH₃ CH₃ NCH₃ Ia1.1711 CF₃ H C₂H₅ NCH₃ Ia1.1712 CF₃ CH₃ C₂H₅ NCH₃ Ia1.1713 CF₃ CH₂CH₃ C₂H₅ NCH₃ Ia1.1714 CF₃ (CH₂)₂CH₃ C₂H₅ NCH₃ Ia1.1715 CF₃ (CH₂)₃CH₃ C₂H₅ NCH₃ Ia1.1716 CF₃ H (CH₂)₂CH₃ NCH₃ Ia1.1717 CF₃ CH₃ (CH₂)₂CH₃ NCH₃ Ia1.1718 CF₃ CH₂CH₃ (CH₂)₂CH₃ NCH₃ Ia1.1719 CF₃ (CH₂)₂CH₃ (CH₂)₂CH₃ NCH₃ Ia1.1720 CF₃ (CH₂)₃CH₃ (CH₂)₂CH₃ NCH₃ Ia1.1721 CF₃ H CH(CH₃)₂ NCH₃ Ia1.1722 CF₃ CH₃ CH(CH₃)₂ NCH₃ Ia1.1723 CF₃ CH₂CH₃ CH(CH₃)₂ NCH₃ Ia1.1724 CF₃ (CH₂)₂CH₃ CH(CH₃)₂ NCH₃ Ia1.1725 CF₃ (CH₂)₃CH₃ CH(CH₃)₂ NCH₃ Ia1.1726 CF₃ H (CH₂)₃CH₃ NCH₃ Ia1.1727 CF₃ CH₃ (CH₂)₃CH₃ NCH₃ Ia1.1728 CF₃ CH₂CH₃ (CH₂)₃CH₃ NCH₃ Ia1.1729 CF₃ (CH₂)₂CH₃ (CH₂)₃CH₃ NCH₃ Ia1.1730 CF₃ (CH₂)₃CH₃ (CH₂)₃CH₃ NCH₃ Ia1.1731 CF₃ H CH₂CH(CH₃)₂ NCH₃ Ia1.1732 CF₃ CH₃ CH₂CH(CH₃)₂ NCH₃ Ia1.1733 CF₃ CH₂CH₃ CH₂CH(CH₃)₂ NCH₃ Ia1.1734 CF₃ (CH₂)₂CH₃ CH₂CH(CH₃)₂ NCH₃ Ia1.1735 CF₃ (CH₂)₃CH₃ CH₂CH(CH₃)₂ NCH₃ Ia1.1736 CF₃ H CH(CH₃)CH₂CH₃ NCH₃ Ia1.1737 CF₃ CH₃ CH(CH₃)CH₂CH₃ NCH₃ Ia1.1738 CF₃ CH₂CH₃ CH(CH₃)CH₂CH₃ NCH₃ Ia1.1739 CF₃ (CH₂)₂CH₃ CH(CH₃)CH₂CH₃ NCH₃ Ia1.1740 CF₃ (CH₂)₃CH₃ CH(CH₃)CH₂CH₃ NCH₃ Ia1.1741 CF₃ H (CH₂)₂—C₆H₅ NCH₃ Ia1.1742 CF₃ CH₃ (CH₂)₂—C₆H₅ NCH₃ Ia1.1743 CF₃ CH₂CH₃ (CH₂)₂—C₆H₅ NCH₃ Ia1.1744 CF₃ (CH₂)₂CH₃ (CH₂)₂—C₆H₅ NCH₃ Ia1.1745 CF₃ (CH₂)₃CH₃ (CH₂)₂—C₆H₅ NCH₃ Ia1.1746 CF₃ H CH₂CH(CH₃)—C₆H₅ NCH₃ Ia1.1747 CF₃ CH₃ CH₂CH(CH₃)—C₆H₅ NCH₃ Ia1.1748 CF₃ CH₂CH₃ CH₂CH(CH₃)—C₆H₅ NCH₃ Ia1.1749 CF₃ (CH₂)₂CH₃ CH₂CH(CH₃)—C₆H₅ NCH₃ Ia1.1750 CF₃ (CH₂)₃CH₃ CH₂CH(CH₃)—C₆H₅ NCH₃ Ia1.1751 CF₃ H CH(CH₃)CH₂—C₆H₅ NCH₃ Ia1.1752 CF₃ CH₃ CH(CH₃)CH₂—C₆H₅ NCH₃ Ia1.1753 CF₃ CH₂CH₃ CH(CH₃)CH₂—C₆H₅ NCH₃ Ia1.1754 CF₃ (CH₂)₂CH₃ CH(CH₃)CH₂—C₆H₅ NCH₃ Ia1.1755 CF₃ (CH₂)₃CH₃ CH(CH₃)CH₂—C₆H₅ NCH₃ Ia1.1756 CF₃ H CH(CH₃)CH(CH₃)—C₆H₅ NCH₃ Ia1.1757 CF₃ CH₃ CH(CH₃)CH(CH₃)—C₆H₅ NCH₃ Ia1.1758 CF₃ CH₂CH₃ CH(CH₃)CH(CH₃)—C₆H₅ NCH₃ Ia1.1759 CF₃ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)—C₆H₅ NCH₃ Ia1.1760 CF₃ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)—C₆H₅ NCH₃ Ia1.1761 CF₃ H (CH₂)₂-(4-Cl—C₆H₄) NCH₃ Ia1.1762 CF₃ CH₃ (CH₂)₂-(4-Cl—C₆H₄) NCH₃ Ia1.1763 CF₃ CH₂CH₃ (CH₂)₂-(4-Cl—C₆H₄) NCH₃ Ia1.1764 CF₃ (CH₂)₂CH₃ (CH₂)₂-(4-Cl—C₆H₄) NCH₃ Ia1.1765 CF₃ (CH₂)₃CH₃ (CH₂)₂-(4-Cl—C₆H₄) NCH₃ Ia1.1766 CF₃ H CH₂CH(CH₃)-(4-Cl—C₆H₄) NCH₃ Ia1.1767 CF₃ CH₃ CH₂CH(CH₃)-(4-Cl—C₆H₄) NCH₃ Ia1.1768 CF₃ CH₂CH₃ CH₂CH(CH₃)-(4-Cl—C₆H₄) NCH₃ Ia1.1769 CF₃ (CH₂)₂CH₃ CH₂CH(CH₃)-(4-Cl—C₆H₄) NCH₃ Ia1.1770 CF₃ (CH₂)₃CH₃ CH₂CH(CH₃)-(4-Cl—C₆H₄) NCH₃ Ia1.1771 CF₃ H CH(CH₃)CH₂-(4-Cl—C₆H₄) NCH₃ Ia1.1772 CF₃ CH₃ CH(CH₃)CH₂-(4-Cl—C₆H₄) NCH₃ Ia1.1773 CF₃ CH₂CH₃ CH(CH₃)CH₂-(4-Cl—C₆H₄) NCH₃ Ia1.1774 CF₃ (CH₂)₂CH₃ CH(CH₃)CH₂-(4-Cl—C₆H₄) NCH₃ Ia1.1775 CF₃ (CH₂)₃CH₃ CH(CH₃)CH₂-(4-Cl—C₆H₄) NCH₃ Ia1.1776 CF₃ H CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) NCH₃ Ia1.1777 CF₃ CH₃ CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) NCH₃ Ia1.1778 CF₃ CH₂CH₃ CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) NCH₃ Ia1.1779 CF₃ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) NCH₃ Ia1.1780 CF₃ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) NCH₃ Ia1.1781 CF₃ H (CH₂)₂-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1782 CF₃ CH₃ (CH₂)₂-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1783 CF₃ CH₂CH₃ (CH₂)₂-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1784 CF₃ (CH₂)₂CH₃ (CH₂)₂-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1785 CF₃ (CH₂)₃CH₃ (CH₂)₂-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1786 CF₃ H CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1787 CF₃ CH₃ CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1788 CF₃ CH₂CH₃ CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1789 CF₃ (CH₂)₂CH₃ CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1790 CF₃ (CH₂)₃CH₃ CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1791 CF₃ H CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1792 CF₃ CH₃ CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1793 CF₃ CH₂CH₃ CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1794 CF₃ (CH₂)₂CH₃ CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1795 CF₃ (CH₂)₃CH₃ CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1796 CF₃ H CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1797 CF₃ CH₃ CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1798 CF₃ CH₂CH₃ CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1799 CF₃ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1800 CF₃ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1801 CF₃ H (CH₂)₂—O—C₆H₅ NCH₃ Ia1.1802 CF₃ CH₃ (CH₂)₂—O—C₆H₅ NCH₃ Ia1.1803 CF₃ CH₂CH₃ (CH₂)₂—O—C₆H₅ NCH₃ Ia1.1804 CF₃ (CH₂)₂CH₃ (CH₂)₂—O—C₆H₅ NCH₃ Ia1.1805 CF₃ (CH₂)₃CH₃ (CH₂)₂—O—C₆H₅ NCH₃ Ia1.1806 CF₃ H CH₂CH(CH₃)—O—C₆H₅ NCH₃ Ia1.1807 CF₃ CH₃ CH₂CH(CH₃)—O—C₆H₅ NCH₃ Ia1.1808 CF₃ CH₂CH₃ CH₂CH(CH₃)—O—C₆H₅ NCH₃ Ia1.1809 CF₃ (CH₂)₂CH₃ CH₂CH(CH₃)—O—C₆H₅ NCH₃ Ia1.1810 CF₃ (CH₂)₃CH₃ CH₂CH (CH₃)—O—C₆H₅ NCH₃ Ia1.1811 CF₃ H CH(CH₃)CH₂—O—C₆H₅ NCH₃ Ia1.1812 CF₃ CH₃ CH(CH₃)CH₂—O—C₆H₅ NCH₃ Ia1.1813 CF₃ CH₂CH₃ CH(CH₃)CH₂—O—C₆H₅ NCH₃ Ia1.1814 CF₃ (CH₂)₂CH₃ CH(CH₃)CH₂—O—C₆H₅ NCH₃ Ia1.1815 CF₃ (CH₂)₃CH₃ CH(CH₃)CH₂—O—C₆H₅ NCH₃ Ia1.1816 CF₃ H CH(CH₃)CH(CH₃)—O—C₆H₅ NCH₃ Ia1.1817 CF₃ CH₃ CH(CH₃)CH(CH₃)—O—C₆H₅ NCH₃ Ia1.1818 CF₃ CH₂CH₃ CH(CH₃)CH(CH₃)—O—C₆H₅ NCH₃ Ia1.1819 CF₃ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)—O—C₆H₅ NCH₃ Ia1.1820 CF₃ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)—O—C₆H₅ NCH₃ Ia1.1821 CF₃ H (CH₂)₂—O-(4-Cl—C₆H₄) NCH₃ Ia1.1822 CF₃ CH₃ (CH₂)₂—O-(4-Cl—C₆H₄) NCH₃ Ia1.1823 CF₃ CH₂CH₃ (CH₂)₂—O-(4-Cl—C₆H₄) NCH₃ Ia1.1824 CF₃ (CH₂)₂CH₃ (CH₂)₂—O-(4-Cl—C₆H₄) NCH₃ Ia1.1825 CF₃ (CH₂)₃CH₃ (CH₂)₂—O-(4-Cl—C₆H₄) NCH₃ Ia1.1826 CF₃ H CH₂CH(CH₃)—O-(4-Cl—C₆H₄) NCH₃ Ia1.1827 CF₃ CH₃ CH₂CH(CH₃)—O-(4-Cl—C₆H₄) NCH₃ Ia1.1828 CF₃ CH₂CH₃ CH₂CH (CH₃)—O-(4-Cl—C₆H₄) NCH₃ Ia1.1829 CF₃ (CH₂)₂CH₃ CH₂CH(CH₃)—O-(4-Cl—C₆H₄) NCH₃ Ia1.1830 CF₃ (CH₂)₃CH₃ CH₂CH(CH₃)—O-(4-Cl—C₆H₄) NCH₃ Ia1.1831 CF₃ H CH(CH₃)CH₂—O-(4-Cl—C₆H₄) NCH₃ Ia1.1832 CF₃ CH₃ CH(CH₃)CH₂—O-(4-Cl—C₆H₄) NCH₃ Ia1.1833 CF₃ CH₂CH₃ CH (CH₃)CH₂—O-(4-Cl—C₆H₄) NCH₃ Ia1.1834 CF₃ (CH₂)₂CH₃ CH(CH₃)CH₂—O-(4-Cl—C₆H₄) NCH₃ Ia1.1835 CF₃ (CH₂)₃CH₃ CH(CH₃)CH₂—O-(4-Cl—C₆H₄) NCH₃ Ia1.1836 CF₃ H CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) NCH₃ Ia1.1837 CF₃ CH₃ CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) NCH₃ Ia1.1838 CF₃ CH₂CH₃ CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) NCH₃ Ia1.1839 CF₃ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) NCH₃ Ia1.1840 CF₃ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) NCH₃ Ia1.1841 CF₃ H (CH₂)₂—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1842 CF₃ CH₃ (CH₂)₂—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1843 CF₃ CH₂CH₃ (CH₂)₂—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1844 CF₃ (CH₂)₂CH₃ (CH₂)₂—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1845 CF₃ (CH₂)₃CH₃ (CH₂)₂—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1846 CF₃ H CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1847 CF₃ CH₃ CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1848 CF₃ CH₂CH₃ CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1849 CF₃ (CH₂)₂CH₃ CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1850 CF₃ (CH₂)₃CH₃ CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1851 CF₃ H CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1852 CF₃ CH₃ CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1853 CF₃ CH₂CH₃ CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1854 CF₃ (CH₂)₂CH₃ CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1855 CF₃ (CH₂)₃CH₃ CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1856 CF₃ H CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1857 CF₃ CH₃ CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1858 CF₃ CH₂CH₃ CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1859 CF₃ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1860 CF₃ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.1861 SO₂CH₃ H CH₃ O Ia1.1862 SO₂CH₃ CH₃ CH₃ O Ia1.1863 SO₂CH₃ CH₂CH₃ CH₃ O Ia1.1864 SO₂CH₃ (CH₂)₂CH₃ CH₃ O Ia1.1865 SO₂CH₃ (CH₂)₃CH₃ CH₃ O Ia1.1866 SO₂CH₃ H C₂H₅ O Ia1.1867 SO₂CH₃ CH₃ C₂H₅ O Ia1.1868 SO₂CH₃ CH₂CH₃ C₂H₅ O Ia1.1869 SO₂CH₃ (CH₂)₂CH₃ C₂H₅ O Ia1.1870 SO₂CH₃ (CH₂)₃CH₃ C₂H₅ O Ia1.1871 SO₂CH₃ H (CH₂)₂CH₃ O Ia1.1872 SO₂CH₃ CH₃ (CH₂)₂CH₃ O Ia1.1873 SO₂CH₃ CH₂CH₃ (CH₂)₂CH₃ O Ia1.1874 SO₂CH₃ (CH₂)₂CH₃ (CH₂)₂CH₃ O Ia1.1875 SO₂CH₃ (CH₂)₃CH₃ (CH₂)₂CH₃ O Ia1.1876 SO₂CH₃ H CH(CH₃)₂ O Ia1.1877 SO₂CH₃ CH₃ CH(CH₃)₂ O Ia1.1878 SO₂CH₃ CH₂CH₃ CH(CH₃)₂ O Ia1.1879 SO₂CH₃ (CH₂)₂CH₃ CH(CH₃)₂ O Ia1.1880 SO₂CH₃ (CH₂)₃CH₃ CH(CH₃)₂ O Ia1.1881 SO₂CH₃ H (CH₂)₃CH₃ O Ia1.1882 SO₂CH₃ CH₃ (CH₂)₃CH₃ O Ia1.1883 SO₂CH₃ CH₂CH₃ (CH₂)₃CH₃ O Ia1.1884 SO₂CH₃ (CH₂)₂CH₃ (CH₂)₃CH₃ O Ia1.1885 SO₂CH₃ (CH₂)₃CH₃ (CH₂)₃CH₃ O Ia1.1886 SO₂CH₃ H CH₂CH(CH₃)₂ O Ia1.1887 SO₂CH₃ CH₃ CH₂CH(CH₃)₂ O Ia1.1888 SO₂CH₃ CH₂CH₃ CH₂CH(CH₃)₂ O Ia1.1889 SO₂CH₃ (CH₂)₂CH₃ CH₂CH(CH₃)₂ O Ia1.1890 SO₂CH₃ (CH₂)₃CH₃ CH₂CH(CH₃)₂ O Ia1.1891 SO₂CH₃ H CH(CH₃)CH₂CH₃ O Ia1.1892 SO₂CH₃ CH₃ CH(CH₃)CH₂CH₃ O Ia1.1893 SO₂CH₃ CH₂CH₃ CH(CH₃)CH₂CH₃ O Ia1.1894 SO₂CH₃ (CH₂)₂CH₃ CH(CH₃)CH₂CH₃ O Ia1.1895 SO₂CH₃ (CH₂)₃CH₃ CH(CH₃)CH₂CH₃ O Ia1.1896 SO₂CH₃ H (CH₂)₂—C₆H₅ O Ia1.1897 SO₂CH₃ CH₃ (CH₂)₂—C₆H₅ O Ia1.1898 SO₂CH₃ CH₂CH₃ (CH₂)₂—C₆H₅ O Ia1.1899 SO₂CH₃ (CH₂)₂CH₃ (CH₂)₂—C₆H₅ O Ia1.1900 SO₂CH₃ (CH₂)₃CH₃ (CH₂)₂—C₆H₅ O Ia1.1901 SO₂CH₃ H CH₂CH(CH₃)—C₆H₅ O Ia1.1902 SO₂CH₃ CH₃ CH₂CH(CH₃)—C₆H₅ O Ia1.1903 SO₂CH₃ CH₂CH₃ CH₂CH(CH₃)—C₆H₅ O Ia1.1904 SO₂CH₃ (CH₂)₂CH₃ CH₂CH(CH₃)—C₆H₅ O Ia1.1905 SO₂CH₃ (CH₂)₃CH₃ CH₂CH(CH₃)—C₆H₅ O Ia1.1906 SO₂CH₃ H CH(CH₃)CH₂—C₆H₅ O Ia1.1907 SO₂CH₃ CH₃ CH(CH₃)CH₂—C₆H₅ O Ia1.1908 SO₂CH₃ CH₂CH₃ CH(CH₃)CH₂—C₆H₅ O Ia1.1909 SO₂CH₃ (CH₂)₂CH₃ CH(CH₃)CH₂—C₆H₅ O Ia1.1910 SO₂CH₃ (CH₂)₃CH₃ CH(CH₃)CH₂—C₆H₅ O Ia1.1911 SO₂CH₃ H CH(CH₃)CH(CH₃)—C₆H₅ O Ia1.1912 SO₂CH₃ CH₃ CH(CH₃)CH(CH₃)—C₆H₅ O Ia1.1913 SO₂CH₃ CH₂CH₃ CH(CH₃)CH(CH₃)—C₆H₅ O Ia1.1914 SO₂CH₃ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)—C₆H₅ O Ia1.1915 SO₂CH₃ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)—C₆H₅ O Ia1.1916 SO₂CH₃ H (CH₂)₂-(4-Cl—C₆H₄) O Ia1.1917 SO₂CH₃ CH₃ (CH₂)₂-(4-Cl—C₆H₄) O Ia1.1918 SO₂CH₃ CH₂CH₃ (CH₂)₂-(4-Cl—C₆H₄) O Ia1.1919 SO₂CH₃ (CH₂)₂CH₃ (CH₂)₂-(4-Cl—C₆H₄) O Ia1.1920 SO₂CH₃ (CH₂)₃CH₃ (CH₂)₂-(4-Cl—C₆H₄) O Ia1.1921 SO₂CH₃ H CH₂CH(CH₃)-(4-Cl—C₆H₄) O Ia1.1922 SO₂CH₃ CH₃ CH₂CH(CH₃)-(4-Cl—C₆H₄) O Ia1.1923 SO₂CH₃ CH₂CH₃ CH₂CH(CH₃)-(4-Cl—C₆H₄) O Ia1.1924 SO₂CH₃ (CH₂)₂CH₃ CH₂CH(CH₃)-(4-Cl—C₆H₄) O Ia1.1925 SO₂CH₃ (CH₂)₃CH₃ CH₂CH(CH₃)-(4-Cl—C₆H₄) O Ia1.1926 SO₂CH₃ H CH(CH₃)CH₂-(4-Cl—C₆H₄) O Ia1.1927 SO₂CH₃ CH₃ CH(CH₃)CH₂-(4-Cl—C₆H₄) O Ia1.1928 SO₂CH₃ CH₂CH₃ CH(CH₃)CH₂-(4-Cl—C₆H₄) O Ia1.1929 SO₂CH₃ (CH₂)₂CH₃ CH(CH₃)CH₂-(4-Cl—C₆H₄) O Ia1.1930 SO₂CH₃ (CH₂)₃CH₃ CH(CH₃)CH₂-(4-Cl—C₆H₄) O Ia1.1931 SO₂CH₃ H CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) O Ia1.1932 SO₂CH₃ CH₃ CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) O Ia1.1933 SO₂CH₃ CH₂CH₃ CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) O Ia1.1934 SO₂CH₃ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) O Ia1.1935 SO₂CH₃ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) O Ia1.1936 SO₂CH₃ H (CH₂)₂-(2,4-Cl₂—C₆H₃) O Ia1.1937 SO₂CH₃ CH₃ (CH₂)₂-(2,4-Cl₂—C₆H₃) O Ia1.1938 SO₂CH₃ CH₂CH₃ (CH₂)₂-(2,4-Cl₂—C₆H₃) O Ia1.1939 SO₂CH₃ (CH₂)₂CH₃ (CH₂)₂-(2,4-Cl₂—C₆H₃) O Ia1.1940 SO₂CH₃ (CH₂)₃CH₃ (CH₂)₂-(2,4-Cl₂—C₆H₃) O Ia1.1941 SO₂CH₃ H CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) O Ia1.1942 SO₂CH₃ CH₃ CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) O Ia1.1943 SO₂CH₃ CH₂CH₃ CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) O Ia1.1944 SO₂CH₃ (CH₂)₂CH₃ CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) Ia1.1945 SO₂CH₃ (CH₂)₃CH₃ CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) O Ia1.1946 SO₂CH₃ H CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) O Ia1.1947 SO₂CH₃ CH₃ CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) O Ia1.1948 SO₂CH₃ CH₂CH₃ CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) O Ia1.1949 SO₂CH₃ (CH₂)₂CH₃ CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) O Ia1.1950 SO₂CH₃ (CH₂)₃CH₃ CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) O Ia1.1951 SO₂CH₃ H CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) O Ia1.1952 SO₂CH₃ CH₃ CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) O Ia1.1953 SO₂CH₃ CH₂CH₃ CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) O Ia1.1954 SO₂CH₃ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) O Ia1.1955 SO₂CH₃ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) O Ia1.1956 SO₂CH₃ H (CH₂)₂—O—C₆H₅ O Ia1.1957 SO₂CH₃ CH₃ (CH₂)₂—O—C₆H₅ O Ia1.1958 SO₂CH₃ CH₂CH₃ (CH₂)₂—O—C₆H₅ O Ia1.1959 SO₂CH₃ (CH₂)₂CH₃ (CH₂)₂—O—C₆H₅ O Ia1.1960 SO₂CH₃ (CH₂)₃CH₃ (CH₂)₂—O—C₆H₅ O Ia1.1961 SO₂CH₃ H CH₂CH(CH₃)—O—C₆H₅ O Ia1.1962 SO₂CH₃ CH₃ CH₂CH(CH₃)—O—C₆H₅ O Ia1.1963 SO₂CH₃ CH₂CH₃ CH₂CH(CH₃)—O—C₆H₅ O Ia1.1964 SO₂CH₃ (CH₂)₂CH₃ CH₂CH(CH₃)—O—C₆H₅ O Ia1.1965 SO₂CH₃ (CH₂)₃CH₃ CH₂CH(CH₃)—O—C₆H₅ O Ia1.1966 SO₂CH₃ H CH(CH₃)CH₂—O—C₆H₅ O Ia1.1967 SO₂CH₃ CH₃ CH(CH₃)CH₂—O—C₆H₅ O Ia1.1968 SO₂CH₃ CH₂CH₃ CH(CH₃)CH₂—O—C₆H₅ O Ia1.1969 SO₂CH₃ (CH₂)₂CH₃ CH(CH₃)CH₂—O—C₆H₅ O Ia1.1970 SO₂CH₃ (CH₂)₃CH₃ CH(CH₃)CH₂—O—C₆H₅ O Ia1.1971 SO₂CH₃ H CH(CH₃)CH(CH₃)—O—C₆H₅ O Ia1.1972 SO₂CH₃ CH₃ CH(CH₃)CH(CH₃)—O—C₆H₅ O Ia1.1973 SO₂CH₃ CH₂CH₃ CH(CH₃)CH(CH₃)—O—C₆H₅ O Ia1.1974 SO₂CH₃ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)—O—C₆H₅ O Ia1.1975 SO₂CH₃ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)—O—C₆H₅ O Ia1.1976 SO₂CH₃ H (CH₂)₂—O-(4-Cl—C₆H₄) O Ia1.1977 SO₂CH₃ CH₃ (CH₂)₂—O-(4-Cl—C₆H₄) O Ia1.1978 SO₂CH₃ CH₂CH₃ (CH₂)₂—O-(4-Cl—C₆H₄) O Ia1.1979 SO₂CH₃ (CH₂)₂CH₃ (CH₂)₂—O-(4-Cl—C₆H₄) O Ia1.1980 SO₂CH₃ (CH₂)₃CH₃ (CH₂)₂—O-(4-Cl—C₆H₄) O Ia1.1981 SO₂CH₃ H CH₂CH(CH₃)—O-(4-Cl—C₆H₄) O Ia1.1982 SO₂CH₃ CH₃ CH₂CH(CH₃)—O-(4-Cl—C₆H₄) O Ia1.1983 SO₂CH₃ CH₂CH₃ CH₂CH(CH₃)—O-(4-Cl—C₆H₄) O Ia1.1984 SO₂CH₃ (CH₂)₂CH₃ CH₂CH(CH₃)—O-(4-Cl—C₆H₄) O Ia1.1985 SO₂CH₃ (CH₂)₃CH₃ CH₂CH(CH₃)—O-(4-Cl—C₆H₄) O Ia1.1986 SO₂CH₃ H CH(CH₃)CH₂—O-(4-Cl—C₆H₄) O Ia1.1987 SO₂CH₃ CH₃ CH(CH₃)CH₂—O-(4-Cl—C₆H₄) O Ia1.1988 SO₂CH₃ CH₂CH₃ CH(CH₃)CH₂—O-(4-Cl—C₆H₄) O Ia1.1989 SO₂CH₃ (CH₂)₂CH₃ CH(CH₃)CH₂—O-(4-Cl—C₆H₄) O Ia1.1990 SO₂CH₃ (CH₂)₃CH₃ CH(CH₃)CH₂—O-(4-Cl—C₆H₄) O Ia1.1991 SO₂CH₃ H CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) O Ia1.1992 SO₂CH₃ CH₃ CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) O Ia1.1993 SO₂CH₃ CH₂CH₃ CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) O Ia1.1994 SO₂CH₃ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) O Ia1.1995 SO₂CH₃ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) O Ia1.1996 SO₂CH₃ H (CH₂)₂—O-(2,4-Cl₂—C₆H₃) O Ia1.1997 SO₂CH₃ CH₃ (CH₂)₂—O-(2,4-Cl₂—C₆H₃) O Ia1.1998 SO₂CH₃ CH₂CH₃ (CH₂)₂—O-(2,4-Cl₂—C₆H₃) O Ia1.1999 SO₂CH₃ (CH₂)₂CH₃ (CH₂)₂—O-(2,4-Cl₂—C₆H₃) O Ia1.2000 SO₂CH₃ (CH₂)₃CH₃ (CH₂)₂—O-(2,4-Cl₂—C₆H₃) O Ia1.2001 SO₂CH₃ H CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) O Ia1.2002 SO₂CH₃ CH₃ CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) O Ia1.2003 SO₂CH₃ CH₂CH₃ CH₂CH(CH₃)—O-(2 ,4-Cl₂—C₆H₃) O Ia1.2004 SO₂CH₃ (CH₂)₂CH₃ CH₂CH(CH₃)—O-( 2 ,4-Cl₂—C₆H₃) O Ia1.2005 SO₂CH₃ (CH₂)₃CH₃ CH₂CH(CH₃)—O-(2 ,4-Cl₂—C₆H₃) O Ia1.2006 SO₂CH₃ H CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) O Ia1.2007 SO₂CH₃ CH₃ CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) O Ia1.2008 SO₂CH₃ CH₂CH₃ CH(CH₃)CH₂—O-(2, 4-Cl₂—C₆H₃) O Ia1.2009 SO₂CH₃ (CH₂)₂CH₃ CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) O Ia1.2010 SO₂CH₃ (CH₂)₃CH₃ CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) O Ia1.2011 SO₂CH₃ H CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) O Ia1.2012 SO₂CH₃ CH₃ CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) O Ia1.2013 SO₂CH₃ CH₂CH₃ CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) O Ia1.2014 SO₂CH₃ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) O Ia1.2015 SO₂CH₃ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) O Ia1.2016 SO₂CH₃ H CH₃ NH Ia1.2017 SO₂CH₃ CH₃ CH₃ NH Ia1.2018 SO₂CH₃ CH₂CH₃ CH₃ NH Ia1.2019 SO₂CH₃ (CH₂)₂CH₃ CH₃ NH Ia1.2020 SO₂CH₃ (CH₂)₃CH₃ CH₃ NH Ia1.2021 SO₂CH₃ H C₂H₅ NH Ia1.2022 SO₂CH₃ CH₃ C₂H₅ NH Ia1.2023 SO₂CH₃ CH₂CH₃ C₂H₅ NH Ia1.2024 SO₂CH₃ (CH₂)₂CH₃ C₂H₅ NH Ia1.2025 SO₂CH₃ (CH₂)₃CH₃ C₂H₅ NH Ia1.2026 SO₂CH₃ H (CH₂)₂CH₃ NH Ia1.2027 SO₂CH₃ CH₃ (CH₂)₂CH₃ NH Ia1.2028 SO₂CH₃ CH₂CH₃ (CH₂)₂CH₃ NH Ia1.2029 SO₂CH₃ (CH₂)₂CH₃ (CH₂)₂CH₃ NH Ia1.2030 SO₂CH₃ (CH₂)₃CH₃ (CH₂)₂CH₃ NH Ia1.2031 SO₂CH₃ H CH(CH₃)₂ NH Ia1.2032 SO₂CH₃ CH₃ CH(CH₃)₂ NH Ia1.2033 SO₂CH₃ CH₂CH₃ CH(CH₃)₂ NH Ia1.2034 SO₂CH₃ (CH₂)₂CH₃ CH(CH₃)₂ NH Ia1.2035 SO₂CH₃ (CH₂)₃CH₃ CH(CH₃)₂ NH Ia1.2036 SO₂CH₃ H (CH₂)₃CH₃ NH Ia1.2037 SO₂CH₃ CH₃ (CH₂)₃CH₃ NH Ia1.2038 SO₂CH₃ CH₂CH₃ (CH₂)₃CH₃ NH Ia1.2039 SO₂CH₃ (CH₂)₂CH₃ (CH₂)₃CH₃ NH Ia1.2040 SO₂CH₃ (CH₂)₃CH₃ (CH₂)₃CH₃ NH Ia1.2041 SO₂CH₃ H CH₂CH(CH₃)₂ NH Ia1.2042 SO₂CH₃ CH₃ CH₂CH(CH₃)₂ NH Ia1.2043 SO₂CH₃ CH₂CH₃ CH₂CH(CH₃)₂ NH Ia1.2044 SO₂CH₃ (CH₂)₂CH₃ CH₂CH(CH₃)₂ NH Ia1.2045 SO₂CH₃ (CH₂)₃CH₃ CH₂CH(CH₃)₂ NH Ia1.2046 SO₂CH₃ H CH(CH₃)CH₂CH₃ NH Ia1.2047 SO₂CH₃ CH₃ CH(CH₃)CH₂CH₃ NH Ia1.2048 SO₂CH₃ CH₂CH₃ CH(CH₃)CH₂CH₃ NH Ia1.2049 SO₂CH₃ (CH₂)₂CH₃ CH(CH₃)CH₂CH₃ NH Ia1.2050 SO₂CH₃ (CH₂)₃CH₃ CH(CH₃)CH₂CH₃ NH Ia1.2051 SO₂CH₃ H (CH₂)₂—C₆H₅ NH Ia1.2052 SO₂CH₃ CH₃ (CH₂)₂—C₆H₅ NH Ia1.2053 SO₂CH₃ CH₂CH₃ (CH₂)₂—C₆H₅ NH Ia1.2054 SO₂CH₃ (CH₂)₂CH₃ (CH₂)₂—C₆H₅ NH Ia1.2055 SO₂CH₃ (CH₂)₃CH₃ (CH₂)₂—C₆H₅ NH Ia1.2056 SO₂CH₃ H CH₂CH(CH₃)—C₆H₅ NH Ia1.2057 SO₂CH₃ CH₃ CH₂CH(CH₃)—C₆H₅ NH Ia1.2058 SO₂CH₃ CH₂CH₃ CH₂CH(CH₃)—C₆H₅ NH Ia1.2059 SO₂CH₃ (CH₂)₂CH₃ CH₂CH(CH₃)—C₆H₅ NH Ia1.2060 SO₂CH₃ (CH₂)₃CH₃ CH₂CH(CH₃)—C₆H₅ NH Ia1.2061 SO₂CH₃ H CH(CH₃)CH₂—C₆H₅ NH Ia1.2062 SO₂CH₃ CH₃ CH(CH₃)CH₂—C₆H₅ NH Ia1.2063 SO₂CH₃ CH₂CH₃ CH(CH₃)CH₂—C₆H₅ NH Ia1.2064 SO₂CH₃ (CH₂)₂CH₃ CH(CH₃)CH₂—C₆H₅ NH Ia1.2065 SO₂CH₃ (CH₂)₃CH₃ CH(CH₃)CH₂—C₆H₅ NH Ia1.2066 SO₂CH₃ H CH(CH₃)CH(CH₃)—C₆H₅ NH Ia1.2067 SO₂CH₃ CH₃ CH(CH₃)CH(CH₃)—C₆H₅ NH Ia1.2068 SO₂CH₃ CH₂CH₃ CH(CH₃)CH(CH₃)—C₆H₅ NH Ia1.2069 SO₂CH₃ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)—C₆H₅ NH Ia1.2070 SO₂CH₃ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)—C₆H₅ NH Ia1.2071 SO₂CH₃ H (CH₂)₂-(4-Cl—C₆H₄) NH Ia1.2072 SO₂CH₃ CH₃ (CH₂)₂-(4-Cl—C₆H₄) NH Ia1.2073 SO₂CH₃ CH₂CH₃ (CH₂)₂-(4-Cl—C₆H₄) NH Ia1.2074 SO₂CH₃ (CH₂)₂CH₃ (CH₂)₂-(4-Cl—C₆H₄) NH Ia1.2075 SO₂CH₃ (CH₂)₃CH₃ (CH₂)₂-(4-Cl—C₆H₄) NH Ia1.2076 SO₂CH₃ H CH₂CH(CH₃)-(4-Cl—C₆H₄) NH Ia1.2077 SO₂CH₃ CH₃ CH₂CH(CH₃)-(4-Cl—C₆H₄) NH Ia1.2078 SO₂CH₃ CH₂CH₃ CH₂CH(CH₃)-(4-Cl—C₆H₄) NH Ia1.2079 SO₂CH₃ (CH₂)₂CH₃ CH₂CH(CH₃)-(4-Cl—C₆H₄) NH Ia1.2080 SO₂CH₃ (CH₂)₃CH₃ CH₂CH(CH₃)-(4-Cl—C₆H₄) NH Ia1.2081 SO₂CH₃ H CH(CH₃)CH₂-(4-Cl—C₆H₄) NH Ia1.2082 SO₂CH₃ CH₃ CH(CH₃)CH₂-(4-Cl—C₆H₄) NH Ia1.2083 SO₂CH₃ CH₂CH₃ CH(CH₃)CH₂-(4-Cl—C₆H₄) NH Ia1.2084 SO₂CH₃ (CH₂)₂CH₃ CH(CH₃)CH₂-(4-Cl—C₆H₄) NH Ia1.2085 SO₂CH₃ (CH₂)₃CH₃ CH(CH₃)CH₂-(4-Cl—C₆H₄) NH Ia1.2086 SO₂CH₃ H CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) NH Ia1.2087 SO₂CH₃ CH₃ CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) NH Ia1.2088 SO₂CH₃ CH₂CH₃ CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) NH Ia1.2089 SO₂CH₃ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) NH Ia1.2090 SO₂CH₃ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) NH Ia1.2091 SO₂CH₃ H (CH₂)₂-(2,4-Cl₂—C₆H₃) NH Ia1.2092 SO₂CH₃ CH₃ (CH₂)₂-(2,4-Cl₂—C₆H₃) NH Ia1.2093 SO₂CH₃ CH₂CH₃ (CH₂)₂-(2,4-Cl₂—C₆H₃) NH Ia1.2094 SO₂CH₃ (CH₂)₂CH₃ (CH₂)₂-(2,4-Cl₂—C₆H₃) NH Ia1.2095 SO₂CH₃ (CH₂)₃CH₃ (CH₂)₂-(2,4-Cl₂—C₆H₃) NH Ia1.2096 SO₂CH₃ H CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) NH Ia1.2097 SO₂CH₃ CH₃ CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) NH Ia1.2098 SO₂CH₃ CH₂CH₃ CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) NH Ia1.2099 SO₂CH₃ (CH₂)₂CH₃ CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) NH Ia1.2100 SO₂CH₃ (CH₂)₃CH₃ CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) NH Ia1.2101 SO₂CH₃ H CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) NH Ia1.2102 SO₂CH₃ CH₃ CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) NH Ia1.2103 SO₂CH₃ CH₂CH₃ CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) NH Ia1.2104 SO₂CH₃ (CH₂)₂CH₃ CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) NH Ia1.2105 SO₂CH₃ (CH₂)₃CH₃ CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) NH Ia1.2106 SO₂CH₃ H CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) NH Ia1.2107 SO₂CH₃ CH₃ CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) NH Ia1.2108 SO₂CH₃ CH₂CH₃ CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) NH Ia1.2109 SO₂CH₃ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) NH Ia1.2110 SO₂CH₃ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) NH Ia1.2111 SO₂CH₃ H (CH₂)₂—O—C₆H₅ NH Ia1.2112 SO₂CH₃ CH₃ (CH₂)₂—O—C₆H₅ NH Ia1.2113 SO₂CH₃ CH₂CH₃ (CH₂)₂—O—C₆H₅ NH Ia1.2114 SO₂CH₃ (CH₂)₂CH₃ (CH₂)₂—O—C₆H₅ NH Ia1.2115 SO₂CH₃ (CH₂)₃CH₃ (CH₂)₂—O—C₆H₅ NH Ia1.2116 SO₂CH₃ H CH₂CH(CH₃)—O—C₆H₅ NH Ia1.2117 SO₂CH₃ CH₃ CH₂CH(CH₃)—O—C₆H₅ NH Ia1.2118 SO₂CH₃ CH₂CH₃ CH₂CH(CH₃)—O—C₆H₅ NH Ia1.2119 SO₂CH₃ (CH₂)₂CH₃ CH₂CH(CH₃)—O—C₆H₅ NH Ia1.2120 SO₂CH₃ (CH₂)₃CH₃ CH₂CH(CH₃)—O—C₆H₅ NH Ia1.2121 SO₂CH₃ H CH(CH₃)CH₂—O—C₆H₅ NH Ia1.2122 SO₂CH₃ CH₃ CH(CH₃)CH₂—O—C₆H₅ NH Ia1.2123 SO₂CH₃ CH₂CH₃ CH(CH₃)CH₂—O—C₆H₅ NH Ia1.2124 SO₂CH₃ (CH₂)₂CH₃ CH(CH₃)CH₂—O—C₆H₅ NH Ia1.2125 SO₂CH₃ (CH₂)₃CH₃ CH(CH₃) CH₂—O—C₆H₅ NH Ia1.2126 SO₂CH₃ H CH(CH₃)CH(CH₃)—O—C₆H₅ NH Ia1.2127 SO₂CH₃ CH₃ CH(CH₃)CH(CH₃)—O—C₆H₅ NH Ia1.2128 SO₂CH₃ CH₂CH₃ CH(CH₃)CH(CH₃)—O—C₆H₅ NH Ia1.2129 SO₂CH₃ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)—O—C₆H₅ NH Ia1.2130 SO₂CH₃ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)—O—C₆H₅ NH Ia1.2131 SO₂CH₃ H (CH₂)₂—O-(4-Cl—C₆H₄) NH Ia1.2132 SO₂CH₃ CH₃ (CH₂)₂—O-(4-Cl—C₆H₄) NH Ia1.2133 SO₂CH₃ CH₂CH₃ (CH₂)₂—O-(4-Cl—C₆H₄) NH Ia1.2134 SO₂CH₃ (CH₂)₂CH₃ (CH₂)₂—O-(4-Cl—C₆H₄) NH Ia1.2135 SO₂CH₃ (CH₂)₃CH₃ (CH₂)₂—O-(4-Cl—C₆H₄) NH Ia1.2136 SO₂CH₃ H CH₂CH(CH₃)—O-(4-Cl—C₆H₄) NH Ia1.2137 SO₂CH₃ CH₃ CH₂CH(CH₃)—O-(4-Cl—C₆H₄) NH Ia1.2138 SO₂CH₃ CH₂CH₃ CH₂CH(CH₃)—O-(4-Cl—C₆H₄) NH Ia1.2139 SO₂CH₃ (CH₂)₂CH₃ CH₂CH(CH₃)—O-(4-Cl—C₆H₄) NH Ia1.2140 SO₂CH₃ (CH₂)₃CH₃ CH₂CH(CH₃)-O-(4-Cl—C₆H₄) NH Ia1.2141 SO₂CH₃ H CH(CH₃)CH₂—O-(4-Cl—C₆H₄) NH Ia1.2142 SO₂CH₃ CH₃ CH(CH₃)CH₂—O-(4-Cl—C₆H₄) NH Ia1.2143 SO₂CH₃ CH₂CH₃ CH(CH₃)CH₂—O-(4-Cl—C₆H₄) NH Ia1.2144 SO₂CH₃ (CH₂)₂CH₃ CH(CH₃)CH₂—O-(4-Cl—C₆H₄) NH Ia1.2145 SO₂CH₃ (CH₂)₃CH₃ CH(CH₃)CH₂—O-(4-Cl—C₆H₄) NH Ia1.2146 SO₂CH₃ H CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) NH Ia1.2147 SO₂CH₃ CH₃ CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) NH Ia1.2148 SO₂CH₃ CH₂CH₃ CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) NH Ia1.2149 SO₂CH₃ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) NH Ia1.2150 SO₂CH₃ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) NH Ia1.2151 SO₂CH₃ H (CH₂)₂—O-(2,4-Cl₂—C₆H₃) NH Ia1.2152 SO₂CH₃ CH₃ (CH₂)₂—O-(2,4-Cl₂—C₆H₃) NH Ia1.2153 SO₂CH₃ CH₂CH₃ (CH₂)₂—O-(2,4-Cl₂—C₆H₃) NH Ia1.2154 SO₂CH₃ (CH₂)₂CH₃ (CH₂)₂—O-(2,4-Cl₂—C₆H₃) NH Ia1.2155 SO₂CH₃ (CH₂)₃CH₃ (CH₂)₂—O-(2,4-Cl₂—C₆H₃) NH Ia1.2156 SO₂CH₃ H CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NH Ia1.2157 SO₂CH₃ CH₃ CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NH Ia1.2158 SO₂CH₃ CH₂CH₃ CH₂CH(CH₃)-O-(2,4-Cl₂—C₆H₃) NH Ia1.2159 SO₂CH₃ (CH₂)₂CH₃ CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NH Ia1.2160 SO₂CH₃ (CH₂)₃CH₃ CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NH Ia1.2161 SO₂CH₃ H CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) NH Ia1.2162 SO₂CH₃ CH₃ CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) NH Ia1.2163 SO₂CH₃ CH₂CH₃ CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) NH Ia1.2164 SO₂CH₃ (CH₂)₂CH₃ CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) NH Ia1.2165 SO₂CH₃ (CH₂)₃CH₃ CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) NH Ia1.2166 SO₂CH₃ H CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NH Ia1.2167 SO₂CH₃ CH₃ CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NH Ia1.2168 SO₂CH₃ CH₂CH₃ CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NH Ia1.2169 SO₂CH₃ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NH Ia1.2170 SO₂CH₃ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NH Ia1.2171 SO₂CH₃ H CH₃ NCH₃ Ia1.2172 SO₂CH₃ CH₃ CH₃ NCH₃ Ia1.2173 SO₂CH₃ CH₂CH₃ CH₃ NCH₃ Ia1.2174 SO₂CH₃ (CH₂)₂CH₃ CH₃ NCH₃ Ia1.2175 SO₂CH₃ (CH₂)₃CH₃ CH₃ NCH₃ Ia1.2176 SO₂CH₃ H C₂H₅ NCH₃ Ia1.2177 SO₂CH₃ CH₃ C₂H₅ NCH₃ Ia1.2178 SO₂CH₃ CH₂CH₃ C₂H₅ NCH₃ Ia1.2179 SO₂CH₃ (CH₂)₂CH₃ C₂H₅ NCH₃ Ia1.2180 SO₂CH₃ (CH₂)₃CH₃ C₂H₅ NCH₃ Ia1.2181 SO₂CH₃ H (CH₂)₂CH₃ NCH₃ Ia1.2182 SO₂CH₃ CH₃ (CH₂)₂CH₃ NCH₃ Ia1.2183 SO₂CH₃ CH₂CH₃ (CH₂)₂CH₃ NCH₃ Ia1.2184 SO₂CH₃ (CH₂)₂CH₃ (CH₂)₂CH₃ NCH₃ Ia1.2185 SO₂CH₃ (CH₂)₃CH₃ (CH₂)₂CH₃ NCH₃ Ia1.2186 SO₂CH₃ H CH(CH₃)₂ NCH₃ Ia1.2187 SO₂CH₃ CH₃ CH(CH₃)₂ NCH₃ Ia1.2188 SO₂CH₃ CH₂CH₃ CH(CH₃)₂ NCH₃ Ia1.2189 SO₂CH₃ (CH₂)₂CH₃ CH(CH₃)₂ NCH₃ Ia1.2190 SO₂CH₃ (CH₂)₃CH₃ CH(CH₃)₂ NCH₃ Ia1.2191 SO₂CH₃ H (CH₂)₃CH₃ NCH₃ Ia1.2192 SO₂CH₃ CH₃ (CH₂)₃CH₃ NCH₃ Ia1.2193 SO₂CH₃ CH₂CH₃ (CH₂)₃CH₃ NCH₃ Ia1.2194 SO₂CH₃ (CH₂)₂CH₃ (CH₂)₃CH₃ NCH₃ Ia1.2195 SO₂CH₃ (CH₂)₃CH₃ (CH₂)₃CH₃ NCH₃ Ia1.2196 SO₂CH₃ H CH₂CH(CH₃)₂ NCH₃ Ia1.2197 SO₂CH₃ CH₃ CH₂CH(CH₃)₂ NCH₃ Ia1.2198 SO₂CH₃ CH₂CH₃ CH₂CH(CH₃)₂ NCH₃ Ia1.2199 SO₂CH₃ (CH₂)₂CH₃ CH₂CH(CH₃)₂ NCH₃ Ia1.2200 SO₂CH₃ (CH₂)₃CH₃ CH₂CH(CH₃)₂ NCH₃ Ia1.2201 SO₂CH₃ H CH(CH₃)CH₂CH₃ NCH₃ Ia1.2202 SO₂CH₃ CH₃ CH(CH₃)CH₂CH₃ NCH₃ Ia1.2203 SO₂CH₃ CH₂CH₃ CH(CH₃)CH₂CH₃ NCH₃ Ia1.2204 SO₂CH₃ (CH₂)₂CH₃ CH(CH₃)CH₂CH₃ NCH₃ Ia1.2205 SO₂CH₃ (CH₂)₃CH₃ CH(CH₃)CH₂CH₃ NCH₃ Ia1.2206 SO₂CH₃ H (CH₂)₂—C₆H₅ NCH₃ Ia1.2207 SO₂CH₃ CH₃ (CH₂)₂—C₆H₅ NCH₃ Ia1.2208 SO₂CH₃ CH₂CH₃ (CH₂)₂—C₆H₅ NCH₃ Ia1.2209 SO₂CH₃ (CH₂)₂CH₃ (CH₂)₂—C₆H₅ NCH₃ Ia1.2210 SO₂CH₃ (CH₂)₃CH₃ (CH₂)₂—C₆H₅ NCH₃ Ia1.2211 SO₂CH₃ H CH₂CH(CH₃)—C₆H₅ NCH₃ Ia1.2212 SO₂CH₃ CH₃ CH₂CH(CH₃)—C₆H₅ NCH₃ Ia1.2213 SO₂CH₃ CH₂CH₃ CH₂CH(CH₃)—C₆H₅ NCH₃ Ia1.2214 SO₂CH₃ (CH₂)₂CH₃ CH₂CH(CH₃)—C₆H₅ NCH₃ Ia1.2215 SO₂CH₃ (CH₂)₃CH₃ CH₂CH(CH₃)—C₆H₅ NCH₃ Ia1.2216 SO₂CH₃ H CH(CH₃)CH₂—C₆H₅ NCH₃ Ia1.2217 SO₂CH₃ CH₃ CH(CH₃)CH₂—C₆H₅ NCH₃ Ia1.2218 SO₂CH₃ CH₂CH₃ CH(CH₃)CH₂—C₆H₅ NCH₃ Ia1.2219 SO₂CH₃ (CH₂)₂CH₃ CH(CH₃)CH₂—C₆H₅ NCH₃ Ia1.2220 SO₂CH₃ (CH₂)₃CH₃ CH(CH₃)CH₂—C₆H₅ NCH₃ Ia1.2221 SO₂CH₃ H CH(CH₃)CH(CH₃)—C₆H₅ NCH₃ Ia1.2222 SO₂CH₃ CH₃ CH(CH₃)CH(CH₃)—C₆H₅ NCH₃ Ia1.2223 SO₂CH₃ CH₂CH₃ CH(CH₃)CH(CH₃)—C₆H₅ NCH₃ Ia1.2224 SO₂CH₃ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)—C₆H₅ NCH₃ Ia1.2225 SO₂CH₃ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)—C₆H₅ NCH₃ Ia1.2226 SO₂CH₃ H (CH₂)₂-(4-Cl—C₆H₄) NCH₃ Ia1.2227 SO₂CH₃ CH₃ (CH₂)₂-(4-Cl—C₆H₄) NCH₃ Ia1.2228 SO₂CH₃ CH₂CH₃ (CH₂)₂-(4-Cl—C₆H₄) NCH₃ Ia1.2229 SO₂CH₃ (CH₂)₂CH₃ (CH₂)₂-(4-Cl—C₆H₄) NCH₃ Ia1.2230 SO₂CH₃ (CH₂)₃CH₃ (CH₂)₂-(4-Cl—C₆H₄) NCH₃ Ia1.2231 SO₂CH₃ H CH₂CH(CH₃)-(4-Cl—C₆H₄) NCH₃ Ia1.2232 SO₂CH₃ CH₃ CH₂CH(CH₃)-(4-Cl—C₆H₄) NCH₃ Ia1.2233 SO₂CH₃ CH₂CH₃ CH₂CH(CH₃)-(4-Cl—C₆H₄) NCH₃ Ia1.2234 SO₂CH₃ (CH₂)₂CH₃ CH₂CH(CH₃)-(4-Cl—C₆H₄) NCH₃ Ia1.2235 SO₂CH₃ (CH₂)₃CH₃ CH₂CH(CH₃)-(4-Cl—C₆H₄) NCH₃ Ia1.2236 SO₂CH₃ H CH(CH₃)CH₂-(4-Cl—C₆H₄) NCH₃ Ia1.2237 SO₂CH₃ CH₃ CH(CH₃)CH₂-(4-Cl—C₆H₄) NCH₃ Ia1.2238 SO₂CH₃ CH₂CH₃ CH(CH₃)CH₂-(4-Cl—C₆H₄) NCH₃ Ia1.2239 SO₂CH₃ (CH₂)₂CH₃ CH(CH₃)CH₂-(4-Cl—C₆H₄) NCH₃ Ia1.2240 SO₂CH₃ (CH₂)₃CH₃ CH(CH₃)CH₂-(4-Cl—C₆H₄) NCH₃ Ia1.2241 SO₂CH₃ H CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) NCH₃ Ia1.2242 SO₂CH₃ CH₃ CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) NCH₃ Ia1.2243 SO₂CH₃ CH₂CH₃ CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) NCH₃ Ia1.2244 SO₂CH₃ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) NCH₃ Ia1.2245 SO₂CH₃ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) NCH₃ Ia1.2246 SO₂CH₃ H (CH₂)₂-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2247 SO₂CH₃ CH₃ (CH₂)₂-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2248 SO₂CH₃ CH₂CH₃ (CH₂)₂-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2249 SO₂CH₃ (CH₂)₂CH₃ (CH₂)₂-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2250 SO₂CH₃ (CH₂)₃CH₃ (CH₂)₂-(214-Cl₂—C₆H₃) NCH₃ Ia1.2251 SO₂CH₃ H CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2252 SO₂CH₃ CH₃ CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2253 SO₂CH₃ CH₂CH₃ CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2254 SO₂CH₃ (CH₂)₂CH₃ CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2255 SO₂CH₃ (CH₂)₃CH₃ CH₂CH(CH₃)-( 2, 4-Cl₂—C₆H₃) NCH₃ Ia1.2256 SO₂CH₃ H CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2257 SO₂CH₃ CH₃ CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2258 SO₂CH₃ CH₂CH₃ CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2259 SO₂CH₃ (CH₂)₂CH₃ CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2260 SO₂CH₃ (CH₂)₃CH₃ CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2261 SO₂CH₃ H CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2262 SO₂CH₃ CH₃ CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2263 SO₂CH₃ CH₂CH₃ CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2264 SO₂CH₃ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2265 SO₂CH₃ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2266 SO₂CH₃ H (CH₂)₂—O—C₆H₅ NCH₃ Ia1.2267 SO₂CH₃ CH₃ (CH₂)₂—O—C₆H₅ NCH₃ Ia1.2268 SO₂CH₃ CH₂CH₃ (CH₂)₂—O—C₆H₅ NCH₃ Ia1.2269 SO₂CH₃ (CH₂)₂CH₃ (CH₂)₂—O—C₆H₅ NCH₃ Ia1.2270 SO₂CH₃ (CH₂)₃CH₃ (CH₂) 2-O—C₆H₅ NCH₃ Ia1.2271 SO₂CH₃ H CH₂CH(CH₃)—O—C₆H₅ NCH₃ Ia1.2272 SO₂CH₃ CH₃ CH₂CH(CH₃)—O—C₆H₅ NCH₃ Ia1.2273 SO₂CH₃ CH₂CH₃ CH₂CH (CH₃)—O—C₆H₅ NCH₃ Ia1.2274 SO₂CH₃ (CH₂)₂CH₃ CH₂CH(CH₃)—O—C₆H₅ NCH₃ Ia1.2275 SO₂CH₃ (CH₂)₃CH₃ CH₂CH(CH₃)—O—C₆H₅ NCH₃ Ia1.2276 SO₂CH₃ H CH(CH₃)CH₂—O—C₆H₅ NCH₃ Ia1.2277 SO₂CH₃ CH₃ CH(CH₃)CH₂—O—C₆H₅ NCH₃ Ia1.2278 SO₂CH₃ CH₂CH₃ CH(CH₃)CH₂—O—C₆H₅ NCH₃ Ia1.2279 SO₂CH₃ (CH₂)₂CH₃ CH(CH₃)CH₂—O—C₆H₅ NCH₃ Ia1.2280 SO₂CH₃ (CH₂)₃CH₃ CH (CH₃)CH₂—O—C₆H₅ NCH₃ Ia1.2281 SO₂CH₃ H CH(CH₃)CH(CH₃)—O—C₆H₅ NCH₃ Ia1.2282 SO₂CH₃ CH₃ CH(CH₃)CH(CH₃)—O—C₆H₅ NCH₃ Ia1.2283 SO₂CH₃ CH₂CH₃ CH(CH₃)CH(CH₃)—O—C₆H₅ NCH₃ Ia1.2284 SO₂CH₃ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)—O—C₆H₅ NCH₃ Ia1.2285 SO₂CH₃ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)—O—C₆H₅ NCH₃ Ia1.2286 SO₂CH₃ H (CH₂)₂—O-(4-Cl—C₆H₄) NCH₃ Ia1.2287 SO₂CH₃ CH₃ (CH₂)₂—O-(4-Cl—C₆H₄) NCH₃ Ia1.2288 SO₂CH₃ CH₂CH₃ (CH₂)₂—O-(4-Cl—C₆H₄) NCH₃ Ia1.2289 SO₂CH₃ (CH₂)₂CH₃ (CH₂)₂—O-(4-Cl—C₆H₄) NCH₃ Ia1.2290 SO₂CH₃ (CH₂)₃CH₃ (CH₂)₂—O-(4-Cl—C₆H₄) NCH₃ Ia1.2291 SO₂CH₃ H CH₂CH(CH₃)—O-(4-Cl—C₆H₄) NCH₃ Ia1.2292 SO₂CH₃ CH₃ CH₂CH(CH₃)—O-(4-Cl—C₆H₄) NCH₃ Ia1.2293 SO₂CH₃ CH₂CH₃ CH₂CH(CH₃)—O-(4-Cl—C₆H₄) NCH₃ Ia1.2294 SO₂CH₃ (CH₂)₂CH₃ CH₂CH(CH₃)—O-(4-Cl—C₆H₄) NCH₃ Ia1.2295 SO₂CH₃ (CH₂)₃CH₃ CH₂CH(CH₃)—O-(4-Cl—C₆H₄) NCH₃ Ia1.2296 SO₂CH₃ H CH(CH₃)CH₂—O-(4-Cl—C₆H₄) NCH₃ Ia1.2297 SO₂CH₃ CH₃ CH(CH₃)CH₂—O-(4-Cl—C₆H₄) NCH₃ Ia1.2298 SO₂CH₃ CH₂CH₃ CH(CH₃)CH₂—O-(4-Cl—C₆H₄) NCH₃ Ia1.2299 SO₂CH₃ (CH₂)₂CH₃ CH(CH₃)CH₂—O-(4-Cl—C₆H₄) NCH₃ Ia1.2300 SO₂CH₃ (CH₂)₃CH₃ CH(CH₃)CH₂—O-(4-Cl—C₆H₄) NCH₃ Ia1.2301 SO₂CH₃ H CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) NCH₃ Ia1.2302 SO₂CH₃ CH₃ CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) NCH₃ Ia1.2303 SO₂CH₃ CH₂CH₃ CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) NCH₃ Ia1.2304 SO₂CH₃ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) NCH₃ Ia1.2305 SO₂CH₃ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) NCH₃ Ia1.2306 SO₂CH₃ H (CH₂)₂—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2307 SO₂CH₃ CH₃ (CH₂)₂—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2308 SO₂CH₃ CH₂CH₃ (CH₂)₂—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2309 SO₂CH₃ (CH₂)₂CH₃ (CH₂)₂—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2310 SO₂CH₃ (CH₂)₃CH₃ (CH₂)₂—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2311 SO₂CH₃ H CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2312 SO₂CH₃ CH₃ CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2313 SO₂CH₃ CH₂CH₃ CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2314 SO₂CH₃ (CH₂)₂CH₃ CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2315 SO₂CH₃ (CH₂)₃CH₃ CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2316 SO₂CH₃ H CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2317 SO₂CH₃ CH₃ CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2318 SO₂CH₃ CH₂CH₃ CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2319 SO₂CH₃ (CH₂)₂CH₃ CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2320 SO₂CH₃ (CH₂)₃CH₃ CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2321 SO₂CH₃ H CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2322 SO₂CH₃ CH₃ CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2323 SO₂CH₃ CH₂CH₃ CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2324 SO₂CH₃ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2325 SO₂CH₃ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2326 NO₂ H CH₃ O Ia1.2327 NO₂ CH₃ CH₃ O Ia1.2328 NO₂ CH₂CH₃ CH₃ O Ia1.2329 NO₂ (CH₂)₂CH₃ CH₃ O Ia1.2330 NO₂ (CH₂)₃CH₃ CH₃ O Ia1.2331 NO₂ H C₂H₅ O Ia1.2332 NO₂ CH₃ C₂H₅ O Ia1.2333 NO₂ CH₂CH₃ C₂H₅ O Ia1.2334 NO₂ (CH₂)₂CH₃ C₂H₅ O Ia1.2335 NO₂ (CH₂)₃CH₃ C₂H₅ O Ia1.2336 NO₂ H (CH₂)₂CH₃ O Ia1.2337 NO₂ CH₃ (CH₂)₂CH₃ O Ia1.2338 NO₂ CH₂CH₃ (CH₂)₂CH₃ O Ia1.2339 NO₂ (CH₂)₂CH₃ (CH₂)₂CH₃ O Ia1.2340 NO₂ (CH₂)₃CH₃ (CH₂)₂CH₃ O Ia1.2341 NO₂ H CH(CH₃)₂ O Ia1.2342 NO₂ CH₃ CH(CH₃)₂ O Ia1.2343 NO₂ CH₂CH₃ CH(CH₃)₂ O Ia1.2344 NO₂ (CH₂)₂CH₃ CH(CH₃)₂ O Ia1.2345 NO₂ (CH₂)₃CH₃ CH(CH₃)₂ O Ia1.2346 NO₂ H (CH₂)₃CH₃ O Ia1.2347 NO₂ CH₃ (CH₂)₃CH₃ O Ia1.2348 NO₂ CH₂CH₃ (CH₂)₃CH₃ O Ia1.2349 NO₂ (CH₂)₂CH₃ (CH₂)₃CH₃ O Ia1.2350 NO₂ (CH₂)₃CH₃ (CH₂)₃CH₃ O Ia1.2351 NO₂ H CH₂CH(CH₃)₂ O Ia1.2352 NO₂ CH₃ CH₂CH(CH₃)₂ O Ia1.2353 NO₂ CH₂CH₃ CH₂CH(CH₃)₂ O Ia1.2354 NO₂ (CH₂)₂CH₃ CH₂CH(CH₃)₂ O Ia1.2355 NO₂ (CH₂)₃CH₃ CH₂CH(CH₃)₂ O Ia1.2356 NO₂ H CH(CH₃)CH₂CH₃ O Ia1.2357 NO₂ CH₃ CH(CH₃)CH₂CH₃ O Ia1.2358 NO₂ CH₂CH₃ CH(CH₃)CH₂CH₃ O Ia1.2359 NO₂ (CH₂)₂CH₃ CH(CH₃)CH₂CH₃ O Ia1.2360 NO₂ (CH₂)₃CH₃ CH(CH₃)CH₂CH₃ O Ia1.2361 NO₂ H (CH₂)₂—C₆H₅ O Ia1.2362 NO₂ CH₃ (CH₂)₂—C₆H₅ O Ia1.2363 NO₂ CH₂CH₃ (CH₂)₂—C₆H₅ O Ia1.2364 NO₂ (CH₂)₂CH₃ (CH₂)₂—C₆H₅ O Ia1.2365 NO₂ (CH₂)₃CH₃ (CH₂)₂—C₆H₅ O Ia1.2366 NO₂ H CH₂CH(CH₃)—C₆H₅ O Ia1.2367 NO₂ CH₃ CH₂CH(CH₃)—C₆H₅ O Ia1.2368 NO₂ CH₂CH₃ CH₂CH(CH₃)—C₆H₅ O Ia1.2369 NO₂ (CH₂)₂CH₃ CH₂CH(CH₃)—C₆H₅ O Ia1.2370 NO₂ (CH₂)₃CH₃ CH₂CH(CH₃)—C₆H₅ O Ia1.2371 NO₂ H CH(CH₃)CH₂—C₆H₅ O Ia1.2372 NO₂ CH₃ CH(CH₃)CH₂—C₆H₅ O Ia1.2373 NO₂ CH₂CH₃ CH(CH₃)CH₂—C₆H₅ O Ia1.2374 NO₂ (CH₂)₂CH₃ CH(CH₃)CH₂—C₆H₅ O Ia1.2375 NO₂ (CH₂)₃CH₃ CH(CH₃)CH₂—C₆H₅ O Ia1.2376 NO₂ H CH(CH₃)CH(CH₃)—C₆H₅ O Ia1.2377 NO₂ CH₃ CH(CH₃)CH(CH₃)—C₆H₅ O Ia1.2378 NO₂ CH₂CH₃ CH(CH₃)CH(CH₃)—C₆H₅ O Ia1.2379 NO₂ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)—C₆H₅ O Ia1.2380 NO₂ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)—C₆H₅ O Ia1.2381 NO₂ H (CH₂)₂-(4-Cl—C₆H₄) O Ia1.2382 NO₂ CH₃ (CH₂)₂-(4-Cl—C₆H₄) O Ia1.2383 NO₂ CH₂CH₃ (CH₂)₂-(4-Cl—C₆H₄) O Ia1.2384 NO₂ (CH₂)₂CH₃ (CH₂)₂-(4-Cl—C₆H₄) O Ia1.2385 NO₂ (CH₂)₃CH₃ (CH₂)₂-(4-Cl—C₆H₄) O Ia1.2386 NO₂ H CH₂CH(CH₃)-(4-Cl—C₆H₄) O Ia1.2387 NO₂ CH₃ CH₂CH(CH₃)-(4-Cl—C₆H₄) O Ia1.2388 NO₂ CH₂CH₃ CH₂CH(CH₃)-(4-Cl—C₆H₄) O Ia1.2389 NO₂ (CH₂)₂CH₃ CH₂CH(CH₃)-(4-Cl—C₆H₄) O Ia1.2390 NO₂ (CH₂)₃CH₃ CH₂CH(CH₃)-(4-Cl—C₆H₄) O Ia1.2391 NO₂ H CH(CH₃)CH₂-(4-Cl—C₆H₄) O Ia1.2392 NO₂ CH₃ CH(CH₃)CH₂-(4-Cl—C₆H₄) O Ia1.2393 NO₂ CH₂CH₃ CH(CH₃)CH₂-(4-Cl—C₆H₄) O Ia1.2394 NO₂ (CH₂)₂CH₃ CH(CH₃)CH₂-(4-Cl—C₆H₄) O Ia1.2395 NO₂ (CH₂)₃CH₃ CH(CH₃)CH₂-(4-Cl—C₆H₄) O Ia1.2396 NO₂ H CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) O Ia1.2397 NO₂ CH₃ CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) O Ia1.2398 NO₂ CH₂CH₃ CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) O Ia1.2399 NO₂ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) O Ia1.2400 NO₂ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) O Ia1.2401 NO₂ H (CH₂)₂-(2,4-Cl₂—C₆H₃) O Ia1.2402 NO₂ CH₃ (CH₂)₂-(2,4-Cl₂—C₆H₃) O Ia1.2403 NO₂ CH₂CH₃ (CH₂)₂-(2,4-Cl₂—C₆H₃) O Ia1.2404 NO₂ (CH₂)₂CH₃ (CH₂)₂-(2,4-Cl₂—C₆H₃) O Ia1.2405 NO₂ (CH₂)₃CH₃ (CH₂)₂-(2,4-Cl₂—C₆H₃) O Ia1.2406 NO₂ H CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) O Ia1.2407 NO₂ CH₃ CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) O Ia1.2408 NO₂ CH₂CH₃ CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) O Ia1.2409 NO₂ (CH₂)₂CH₃ CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) O Ia1.2410 NO₂ (CH₂)₃CH₃ CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) O Ia1.2411 NO₂ H CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) O Ia1.2412 NO₂ CH₃ CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) O Ia1.2413 NO₂ CH₂CH₃ CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) O Ia1.2414 NO₂ (CH₂)₂CH₃ CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) O Ia1.2415 NO₂ (CH₂)₃CH₃ CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) O Ia1.2416 NO₂ H CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) O Ia1.2417 NO₂ CH₃ CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) O Ia1.2418 NO₂ CH₂CH₃ CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) O Ia1.2419 NO₂ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) O Ia1.2420 NO₂ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) O Ia1.2421 NO₂ H (CH₂)₂—O—C₆H₅ O Ia1.2422 NO₂ CH₃ (CH₂)₂—O—C₆H₅ O Ia1.2423 NO₂ CH₂CH₃ (CH₂)₂—O—C₆H₅ O Ia1.2424 NO₂ (CH₂)₂CH₃ (CH₂)₂—O—C₆H₅ O Ia1.2425 NO₂ (CH₂)₃CH₃ (CH₂)₂—O—C₆H₅ O Ia1.2426 NO₂ H CH₂CH(CH₃)—O—C₆H₅ O Ia1.2427 NO₂ CH₃ CH₂CH(CH₃)—O—C₆H₅ O Ia1.2428 NO₂ CH₂CH₃ CH₂CH(CH₃)—O—C₆H₅ O Ia1.2429 NO₂ (CH₂)₂CH₃ CH₂CH(CH₃)—O—C₆H₅ O Ia1.2430 NO₂ (CH₂)₃CH₃ CH₂CH(CH₃)—O—C₆H₅ O Ia1.2431 NO₂ H CH(CH₃)CH₂—O—C₆H₅ O Ia1.2432 NO₂ CH₃ CH(CH₃)CH₂—O—C₆H₅ O Ia1.2433 NO₂ CH₂CH₃ CH(CH₃)CH₂—O—C₆H₅ O Ia1.2434 NO₂ (CH₂)₂CH₃ CH(CH₃)CH₂—O—C₆H₅ O Ia1.2435 NO₂ (CH₂)₃CH₃ CH(CH₃)CH₂—O—C₆H₅ O Ia1.2436 NO₂ H CH(CH₃)CH(CH₃)—O—C₆H₅ O Ia1.2437 NO₂ CH₃ CH(CH₃)CH(CH₃)—O—C₆H₅ O Ia1.2438 NO₂ CH₂CH₃ CH(CH₃)CH(CH₃)—O—C₆H₅ O Ia1.2439 NO₂ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)—O—C₆H₅ O Ia1.2440 NO₂ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)—O—C₆H₅ O Ia1.2441 NO₂ H (CH₂)₂—O-(4-Cl—C₆H₄) O Ia1.2442 NO₂ CH₃ (CH₂)₂—O-(4-Cl—C₆H₄) O Ia1.2443 NO₂ CH₂CH₃ (CH₂)₂—O-(4-Cl—C₆H₄) O Ia1.2444 NO₂ (CH₂)₂CH₃ (CH₂)₂—O-(4-Cl—C₆H₄) O Ia1.2445 NO₂ (CH₂)₃CH₃ (CH₂)₂—O-(4-Cl—C₆H₄) O Ia1.2446 NO₂ H CH₂CH(CH₃)—O-(4-Cl—C₆H₄) O Ia1.2447 NO₂ CH₃ CH₂CH(CH₃)—O-(4-Cl—C₆H₄) O Ia1.2448 NO₂ CH₂CH₃ CH₂CH(CH₃)—O-(4-Cl—C₆H₄) O Ia1.2449 NO₂ (CH₂)₂CH₃ CH₂CH(CH₃)—O-(4-Cl—C₆H₄) O Ia1.2450 NO₂ (CH₂)₃CH₃ CH₂CH(CH₃)—O-(4-Cl—C₆H₄) O Ia1.2451 NO₂ H CH(CH₃)CH₂—O-(4-Cl—C₆H₄) O Ia1.2452 NO₂ CH₃ CH(CH₃)CH₂—O-(4-Cl—C₆H₄) O Ia1.2453 NO₂ CH₂CH₃ CH(CH₃)CH₂—O-(4-Cl—C₆H₄) O Ia1.2454 NO₂ (CH₂)₂CH₃ CH(CH₃)CH₂—O-(4-Cl—C₆H₄) O Ia1.2455 NO₂ (CH₂)₃CH₃ CH(CH₃)CH₂—O-(4-Cl—C₆H₄) O Ia1.2456 NO₂ H CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) O Ia1.2457 NO₂ CH₃ CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) O Ia1.2458 NO₂ CH₂CH₃ CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) O Ia1.2459 NO₂ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) O Ia1.2460 NO₂ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) O Ia1.2461 NO₂ H (CH₂)₂—O-(2,4-Cl₂—C₆H₃) O Ia1.2462 NO₂ CH₃ (CH₂)₂—O-(2,4-Cl₂—C₆H₃) O Ia1.2463 NO₂ CH₂CH₃ (CH₂)₂—O-(2,4-Cl₂—C₆H₃) O Ia1.2464 NO₂ (CH₂)₂CH₃ (CH₂)₂—O-(2,4-Cl₂—C₆H₃) O Ia1.2465 NO₂ (CH₂)₃CH₃ (CH₂)₂—O-(2,4-Cl₂—C₆H₃) O Ia1.2466 NO₂ H CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) O Ia1.2467 NO₂ CH₃ CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) O Ia1.2468 NO₂ CH₂CH₃ CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) O Ia1.2469 NO₂ (CH₂)₂CH₃ CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) O Ia1.2470 NO₂ (CH₂)₃CH₃ CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) O Ia1.2471 NO₂ H CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) O Ia1.2472 NO₂ CH₃ CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) O Ia1.2473 NO₂ CH₂CH₃ CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) O Ia1.2474 NO₂ (CH₂)₂CH₃ CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) O Ia1.2475 NO₂ (CH₂)₃CH₃ CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) O Ia1.2476 NO₂ H CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) O Ia1.2477 NO₂ CH₃ CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) O Ia1.2478 NO₂ CH₂CH₃ CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) O Ia1.2479 NO₂ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) O Ia1.2480 NO₂ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) O Ia1.2481 NO₂ H CH₃ NH Ia1.2482 NO₂ CH₃ CH₃ NH Ia1.2483 NO₂ CH₂CH₃ CH₃ NH Ia1.2484 NO₂ (CH₂)₂CH₃ CH₃ NH Ia1.2485 NO₂ (CH₂)₃CH₃ CH₃ NH Ia1.2486 NO₂ H C₂H₅ NH Ia1.2487 NO₂ CH₃ C₂H₅ NH Ia1.2488 NO₂ CH₂CH₃ C₂H₅ NH Ia1.2489 NO₂ (CH₂)₂CH₃ C₂H₅ NH Ia1.2490 NO₂ (CH₂)₃CH₃ C₂H₅ NH Ia1.2491 NO₂ H (CH₂)₂CH₃ NH Ia1.2492 NO₂ CH₃ (CH₂)₂CH₃ NH Ia1.2493 NO₂ CH₂CH₃ (CH₂)₂CH₃ NH Ia1.2494 NO₂ (CH₂)₂CH₃ (CH₂)₂CH₃ NH Ia1.2495 NO₂ (CH₂)₃CH₃ (CH₂)₂CH₃ NH Ia1.2496 NO₂ H CH(CH₃)₂ NH Ia1.2497 NO₂ CH₃ CH(CH₃)₂ NH Ia1.2498 NO₂ CH₂CH₃ CH(CH₃)₂ NH Ia1.2499 NO₂ (CH₂)₂CH₃ CH(CH₃)₂ NH Ia1.2500 NO₂ (CH₂)₃CH₃ CH(CH₃)₂ NH Ia1.2501 NO₂ H (CH₂)₃CH₃ NH Ia1.2502 NO₂ CH₃ (CH₂)₃CH₃ NH Ia1.2503 NO₂ CH₂CH₃ (CH₂)₃CH₃ NH Ia1.2504 NO₂ (CH₂)₂CH₃ (CH₂)₃CH₃ NH Ia1.2505 NO₂ (CH₂)₃CH₃ (CH₂)₃CH₃ NH Ia1.2506 NO₂ H CH₂CH(CH₃)₂ NH Ia1.2507 NO₂ CH₃ CH₂CH(CH₃)₂ NH Ia1.2508 NO₂ CH₂CH₃ CH₂CH(CH₃)₂ NH Ia1.2509 NO₂ (CH₂)₂CH₃ CH₂CH(CH₃)₂ NH Ia1.2510 NO₂ (CH₂)₃CH₃ CH₂CH(CH₃)₂ NH Ia1.2511 NO₂ H CH(CH₃)CH_(2CH) ₃ NH Ia1.2512 NO₂ CH₃ CH(CH₃)CH₂CH₃ NH Ia1.2513 NO₂ CH₂CH₃ CH(CH₃)CH₂CH₃ NH Ia1.2514 NO₂ (CH₂)₂CH₃ CH(CH₃)CH₂CH₃ NH Ia1.2515 NO₂ (CH₂)₃CH₃ CH(CH₃)CH₂CH₃ NH Ia1.2516 NO₂ H (CH₂)₂—C₆H₅ NH Ia1.2517 NO₂ CH₃ (CH₂)₂—C₆H₅ NH Ia1.2518 NO₂ CH₂CH₃ (CH₂)₂—C₆H₅ NH Ia1.2519 NO₂ (CH₂)₂CH₃ (CH₂)₂—C₆H₅ NH Ia1.2520 NO₂ (CH₂)₃CH₃ (CH₂)₂—C₆H₅ NH Ia1.2521 NO₂ H CH₂CH(CH₃)—C₆H₅ NH Ia1.2522 NO₂ CH₃ CH₂CH(CH₃)—C₆H₅ NH Ia1.2523 NO₂ CH₂CH₃ CH₂CH(CH₃)—C₆H₅ NH Ia1.2524 NO₂ (CH₂)₂CH₃ CH₂CH(CH₃)—C₆H₅ NH Ia1.2525 NO₂ (CH₂)₃CH₃ CH₂CH(CH₃)—C₆H₅ NH Ia1.2526 NO₂ H CH(CH₃)CH₂—C₆H₅ NH Ia1.2527 NO₂ CH₃ CH(CH₃)CH₂—C₆H₅ NH Ia1.2528 NO₂ CH₂CH₃ CH(CH₃)CH₂—C₆H₅ NH Ia1.2529 NO₂ (CH₂)₂CH₃ CH(CH₃)CH₂—C₆H₅ NH Ia1.2530 NO₂ (CH₂)₃CH₃ CH(CH₃)CH₂—C₆H₅ NH Ia1.2531 NO₂ H CH(CH₃)CH(CH₃)—C₆H₅ NH Ia1.2532 NO₂ CH₃ CH(CH₃)CH(CH₃)—C₆H₅ NH Ia1.2533 NO₂ CH₂CH₃ CH(CH₃)CH(CH₃)—C₆H₅ NH Ia1.2534 NO₂ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)—C₆H₅ NH Ia1.2535 NO₂ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)—C₆H₅ NH Ia1.2536 NO₂ H (CH₂)₂-(4-Cl—C₆H₄) NH Ia1.2537 NO₂ CH₃ (CH₂)₂-(4-Cl—C₆H₄) NH Ia1.2538 NO₂ CH₂CH₃ (CH₂)₂-(4-Cl—C₆H₄) NH Ia1.2539 NO₂ (CH₂)₂CH₃ (CH₂)₂-(4-Cl—C₆H₄) NH Ia1.2540 NO₂ (CH₂)₃CH₃ (CH₂)₂-(4-Cl—C₆H₄) NH Ia1.2541 NO₂ H CH₂CH(CH₃)-(4-Cl—C₆H₄) NH Ia1.2542 NO₂ CH₃ CH₂CH(CH₃)-(4-Cl—C₆H₄) NH Ia1.2543 NO₂ CH₂CH₃ CH₂CH(CH₃)-(4-Cl—C₆H₄) NH Ia1.2544 NO₂ (CH₂)₂CH₃ CH₂CH(CH₃)-(4-Cl—C₆H₄) NH Ia1.2545 NO₂ (CH₂)₃CH₃ CH₂CH(CH₃)-(4-Cl—C₆H₄) NH Ia1.2546 NO₂ H CH(CH₃)CH₂-(4-Cl—C₆H₄) NH Ia1.2547 NO₂ CH₃ CH(CH₃)CH₂-(4-Cl—C₆H₄) NH Ia1.2548 NO₂ CH₂CH₃ CH(CH₃)CH₂-(4-Cl—C₆H₄) NH Ia1.2549 NO₂ (CH₂)₂CH₃ CH(CH₃)CH₂-(4-Cl—C₆H₄) NH Ia1.2550 NO₂ (CH₂)₃CH₃ CH(CH₃)CH₂-(4-Cl—C₆H₄) NH Ia1.2551 NO₂ H CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) NH Ia1.2552 NO₂ CH₃ CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) NH Ia1.2553 NO₂ CH₂CH₃ CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) NH Ia1.2554 NO₂ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) NH Ia1.2555 NO₂ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) NH Ia1.2556 NO₂ H (CH₂)₂-(2,4-Cl₂—C₆H₃) NH Ia1.2557 NO₂ CH₃ (CH₂)₂-(2,4-Cl₂—C₆H₃) NH Ia1.2558 NO₂ CH₂CH₃ (CH₂)₂-(2,4-Cl₂—C₆H₃) NH Ia1.2559 NO₂ (CH₂)₂CH₃ (CH₂)₂-(2,4-Cl₂—C₆H₃) NH Ia1.2560 NO₂ (CH₂)₃CH₃ (CH₂)₂-(2,4-Cl₂—C₆H₃) NH Ia1.2561 NO₂ H CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) NH Ia1.2562 NO₂ CH₃ CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) NH Ia1.2563 NO₂ CH₂CH₃ CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) NH Ia1.2564 NO₂ (CH₂)₂CH₃ CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) NH Ia1.2565 NO₂ (CH₂)₃CH₃ CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) NH Ia1.2566 NO₂ H CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) NH Ia1.2567 NO₂ CH₃ CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) NH Ia1.2568 NO₂ CH₂CH₃ CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) NH Ia1.2569 NO₂ (CH₂)₂CH₃ CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) NH Ia1.2570 NO₂ (CH₂)₃CH₃ CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) NH Ia1.2571 NO₂ H CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) NH Ia1.2572 NO₂ CH₃ CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) NH Ia1.2573 NO₂ CH₂CH₃ CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) NH Ia1.2574 NO₂ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) NH Ia1.2575 NO₂ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) NH Ia1.2576 NO₂ H (CH₂)₂—O—C₆H₅ NH Ia1.2577 NO₂ CH₃ (CH₂)₂—O—C₆H₅ NH Ia1.2578 NO₂ CH₂CH₃ (CH₂)₂—O—C₆H₅ NH Ia1.2579 NO₂ (CH₂)₂CH₃ (CH₂)₂—O—C₆H₅ NH Ia1.2580 NO₂ (CH₂)₃CH₃ (CH₂)₂—O—C₆H₅ NH Ia1.2581 NO₂ H CH₂CH(CH₃)—O—C₆H₅ NH Ia1.2582 NO₂ CH₃ CH₂CH(CH₃)—O—C₆H₅ NH Ia1.2583 NO₂ CH₂CH₃ CH₂CH(CH₃)—O—C₆H₅ NH Ia1.2584 NO₂ (CH₂)₂CH₃ CH₂CH(CH₃)—O—C₆H₅ NH Ia1.2585 NO₂ (CH₂)₃CH₃ CH₂CH(CH₃)—O—C₆H₅ NH Ia1.2586 NO₂ H CH(CH₃)CH₂—O—C₆H₅ NH Ia1.2587 NO₂ CH₃ CH(CH₃)CH₂—O—C₆H₅ NH Ia1.2588 NO₂ CH₂CH₃ CH(CH₃)CH₂—O—C₆H₅ NH Ia1.2589 NO₂ (CH₂)₂CH₃ CH(CH₃)CH₂—O—C₆H₅ NH Ia1.2590 NO₂ (CH₂)₃CH₃ CH(CH₃)CH₂—O—C₆H₅ NH Ia1.2591 NO₂ H CH(CH₃)CH(CH₃)—O—C₆H₅ NH Ia1.2592 NO₂ CH₃ CH(CH₃)CH(CH₃)—O—C₆H₅ NH Ia1.2593 NO₂ CH₂CH₃ CH(CH₃)CH(CH₃)—O—C₆H₅ NH Ia1.2594 NO₂ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)—O—C₆H₅ NH Ia1.2595 NO₂ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)—O—C₆H₅ NH Ia1.2596 NO₂ H (CH₂)₂—O-(4-Cl—C₆H₄) NH Ia1.2597 NO₂ CH₃ (CH₂)₂—O-(4-Cl—C₆H₄) NH Ia1.2598 NO₂ CH₂CH₃ (CH₂)₂—O-(4-Cl—C₆H₄) NH Ia1.2599 NO₂ (CH₂)₂CH₃ (CH₂)₂—O-(4-Cl—C₆H₄) NH Ia1.2600 NO₂ (CH₂)₃CH₃ (CH₂)₂—O-(4-Cl—C₆H₄) NH Ia1.2601 NO₂ H CH₂CH(CH₃)—O-(4-Cl—C₆H₄) NH Ia1.2602 NO₂ CH₃ CH₂CH(CH₃)—O-(4-Cl—C₆H₄) NH Ia1.2603 NO₂ CH₂CH₃ CH₂CH(CH₃)—O-(4-Cl—C₆H₄) NH Ia1.2604 NO₂ (CH₂)₂CH₃ CH₂CH(CH₃)—O-(4-Cl—C₆H₄) NH Ia1.2605 NO₂ (CH₂)₃CH₃ CH₂CH(CH₃)—O-(4-Cl—C₆H₄) NH Ia1.2606 NO₂ H CH(CH₃)CH₂—O-(4-Cl—C₆H₄) NH Ia1.2607 NO₂ CH₃ CH(CH₃)CH₂—O-(4-Cl—C₆H₄) NH Ia1.2608 NO₂ CH₂CH₃ CH(CH₃)CH₂—O-(4-Cl—C₆H₄) NH Ia1.2609 NO₂ (CH₂)₂CH₃ CH(CH₃)CH₂—O-(4-Cl—C₆H₄) NH Ia1.2610 NO₂ (CH₂)₃CH₃ CH(CH₃)CH₂—O-(4-Cl—C₆H₄) NH Ia1.2611 NO₂ H CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) NH Ia1.2612 NO₂ CH₃ CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) NH Ia1.2613 NO₂ CH₂CH₃ CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) NH Ia1.2614 NO₂ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) NH Ia1.2615 NO₂ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) NH Ia1.2616 NO₂ H (CH₂)₂—O-(2,4-Cl₂—C₆H₃) NH Ia1.2617 NO₂ CH₃ (CH₂)₂—O-(2,4-Cl₂—C₆H₃) NH Ia1.2618 NO₂ CH₂CH₃ (CH₂)₂—O-(2,4-Cl₂—C₆H₃) NH Ia1.2619 NO₂ (CH₂)₂CH₃ (CH₂)₂—O-(2,4-Cl₂—C₆H₃) NH Ia1.2620 NO₂ (CH₂)₃CH₃ (CH₂)₂—O-(2,4-Cl₂—C₆H₃) NH Ia1.2621 NO₂ H CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NH Ia1.2622 NO₂ CH₃ CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NH Ia1.2623 NO₂ CH₂CH₃ CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NH Ia1.2624 NO₂ (CH₂)₂CH₃ CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NH Ia1.2625 NO₂ (CH₂)₃CH₃ CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NH Ia1.2626 NO₂ H CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) NH Ia1.2627 NO₂ CH₃ CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) NH Ia1.2628 NQ2 CH₂CH₃ CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) NH Ia1.2629 NO₂ (CH₂)₂CH₃ CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) NH Ia1.2630 NO₂ (CH₂)₃CH₃ CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) NH Ia1.2631 NO₂ H CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NH Ia1.2632 NO₂ CH₃ CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NH Ia1.2633 NO₂ CH₂CH₃ CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NH Ia1.2634 NO₂ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NH Ia1.2635 NO₂ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NH Ia1.2636 NO₂ H CH₃ NCH₃ Ia1.2637 NO₂ CH₃ CH₃ NCH₃ Ia1.2638 NO₂ CH₂CH₃ CH₃ NCH₃ Ia1.2639 NO₂ (CH₂)₂CH₃ CH₃ NCH₃ Ia1.2640 NO₂ (CH₂)₃CH₃ CH₃ NCH₃ Ia1.2641 NO₂ H C₂H₅ NCH₃ Ia1.2642 NO₂ CH₃ C₂H₅ NCH₃ Ia1.2643 NO₂ CH₂CH₃ C₂H₅ NCH₃ Ia1.2644 NO₂ (CH₂)₂CH₃ C₂H₅ NCH₃ Ia1.2645 NO₂ (CH₂)₃CH₃ C₂H₅ NCH₃ Ia1.2646 NO₂ H (CH₂)₂CH₃ NCH₃ Ia1.2647 NO₂ CH₃ (CH₂)₂CH₃ NCH₃ Ia1.2648 NO₂ CH₂CH₃ (CH₂)₂CH₃ NCH₃ Ia1.2649 NO₂ (CH₂)₂CH₃ (CH₂)₂CH₃ NCH₃ Ia1.2650 NO₂ (CH₂)₃CH₃ (CH₂)₂CH₃ NCH₃ Ia1.2651 NO₂ H CH(CH₃)₂ NCH₃ Ia1.2652 NO₂ CH₃ CH(CH₃)₂ NCH₃ Ia1.2653 NO₂ CH₂CH₃ CH(CH₃)₂ NCH₃ Ia1.2654 NO₂ (CH₂)₂CH₃ CH(CH₃)₂ NCH₃ Ia1.2655 NO₂ (CH₂)₃CH₃ CH(CH₃)₂ NCH₃ Ia1.2656 NO₂ H (CH₂)₃CH₃ NCH₃ Ia1.2657 NO₂ CH₃ (CH₂)₃CH₃ NCH₃ Ia1.2658 NO₂ CH₂CH₃ (CH₂)₃CH₃ NCH₃ Ia1.2659 NO₂ (CH₂)₂CH₃ (CH₂)₃CH₃ NCH₃ Ia1.2660 NO₂ (CH₂)₃CH₃ (CH₂)₃CH₃ NCH₃ Ia1.2661 NO₂ H CH₂CH(CH₃)₂ NCH₃ Ia1.2662 NO₂ CH₃ CH₂CH(CH₃)₂ NCH₃ Ia1.2663 NO₂ CH₂CH₃ CH₂CH(CH₃)₂ NCH₃ Ia1.2664 NO₂ (CH₂)₂CH₃ CH₂CH(CH₃)₂ NCH₃ Ia1.2665 NO₂ (CH₂)₃CH₃ CH₂CH(CH₃)₂ NCH₃ Ia1.2666 NO₂ H CH(CH₃)CH₂CH₃ NCH₃ Ia1.2667 NO₂ CH₃ CH(CH₃)CH₂CH₃ NCH₃ Ia1.2668 NO₂ CH₂CH₃ CH(CH₃)CH₂CH₃ NCH₃ Ia1.2669 NO₂ (CH₂)₂CH₃ CH(CH₃)CH₂CH₃ NCH₃ Ia1.2670 NO₂ (CH₂)₃CH₃ CH(CH₃)CH₂CH₃ NCH₃ Ia1.2671 NO₂ H (CH₂)₂—C₆H₅ NCH₃ Ia1.2672 NO₂ CH₃ (CH₂)₂—C₆H₅ NCH₃ Ia1.2673 NO₂ CH₂CH₃ (CH₂)₂—C₆H₅ NCH₃ Ia1.2674 NO₂ (CH₂)₂CH₃ (CH₂)₂—C₆H₅ NCH₃ Ia1.2675 NO₂ (CH₂)₃CH₃ (CH₂)₂—C₆H₅ NCH₃ Ia1.2676 NO₂ H CH₂CH(CH₃)—C₆H₅ NCH₃ Ia1.2677 NO₂ CH₃ CH₂CH(CH₃)—C₆H₅ NCH₃ Ia1.2678 NO₂ CH₂CH₃ CH₂CH(CH₃)—C₆H₅ NCH₃ Ia1.2679 NO₂ (CH₂)₂CH₃ CH₂CH(CH₃)—C₆H₅ NCH₃ Ia1.2680 NO₂ (CH₂)₃CH₃ CH₂CH(CH₃)—C₆H₅ NCH₃ Ia1.2681 NO₂ H CH(CH₃)CH₂—C₆H₅ NCH₃ Ia1.2682 NO₂ CH₃ CH(CH₃)CH₂—C₆H₅ NCH₃ Ia1.2683 NO₂ CH₂CH₃ CH(CH₃)CH₂—C₆H₅ NCH₃ Ia1.2684 NO₂ (CH₂)₂CH₃ CH(CH₃)CH₂—C₆H₅ NCH₃ Ia1.2685 NO₂ (CH₂)₃CH₃ CH(CH₃)CH₂—C₆H₅ NCH₃ Ia1.2686 NO₂ H CH(CH₃)CH(CH₃)—C₆H₅ NCH₃ Ia1.2687 NO₂ CH₃ CH(CH₃)CH(CH₃)—C₆H₅ NCH₃ Ia1.2688 NO₂ CH₂CH₃ CH(CH₃)CH(CH₃)—C₆H₅ NCH₃ Ia1.2689 NO₂ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)—C₆H₅ NCH₃ Ia1.2690 NO₂ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)—C₆H₅ NCH₃ Ia1.2691 NO₂ H (CH₂)₂-(4-Cl—C₆H₄) NCH₃ Ia1.2692 NO₂ CH₃ (CH₂)₂-(4-Cl—C₆H₄) NCH₃ Ia1.2693 NO₂ CH₂CH₃ (CH₂)₂-(4-Cl—C₆H₄) NCH₃ Ia1.2694 NO₂ (CH₂)₂CH₃ (CH₂)₂-(4-Cl—C₆H₄) NCH₃ Ia1.2695 NO₂ (CH₂)₃CH₃ (CH₂)₂-(4-Cl—C₆H₄) NCH₃ Ia1.2696 NO₂ H CH₂CH(CH₃)-(4-Cl—C₆H₄) NCH₃ Ia1.2697 NO₂ CH₃ CH₂CH(CH₃)-(4-Cl—C₆H₄) NCH₃ Ia1.2698 NO₂ CH₂CH₃ CH₂CH(CH₃)-(4-Cl—C₆H₄) NCH₃ Ia1.2699 NO₂ (CH₂)₂CH₃ CH₂CH(CH₃)-(4-Cl—C₆H₄) NCH₃ Ia1.2700 NO₂ (CH₂)₃CH₃ CH₂CH(CH₃)-(4-Cl—C₆H₄) NCH₃ Ia1.2701 NO₂ H CH(CH₃)CH₂-(4-Cl—C₆H₄) NCH₃ Ia1.2702 NO₂ CH₃ CH(CH₃)CH₂-(4-Cl—C₆H₄) NCH₃ Ia1.2703 NO₂ CH₂CH₃ CH(CH₃)CH₂-(4-Cl—C₆H₄) NCH₃ Ia1.2704 NO₂ (CH₂)₂CH₃ CH(CH₃)CH₂-(4-Cl—C₆H₄) NCH₃ Ia1.2705 NO₂ (CH₂)₃CH₃ CH(CH₃)CH₂-(4-Cl—C₆H₄) NCH₃ Ia1.2706 NO₂ H CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) NCH₃ Ia1.2707 NO₂ CH₃ CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) NCH₃ Ia1.2708 NO₂ CH₂CH₃ CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) NCH₃ Ia1.2709 NO₂ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) NCH₃ Ia1.2710 N62 (CH₂)₃CH₃ CH(CH₃)CH(CH₃)-(4-Cl—C₆H₄) NCH₃ Ia1.2711 NO₂ H (CH₂)₂-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2712 NO₂ CH₃ (CH₂)₂-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2713 NO₂ CH₂CH₃ (CH₂)₂-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2714 NO₂ (CH₂)₂CH₃ (CH₂)₂-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2715 NO₂ (CH₂)₃CH₃ (CH₂)₂-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2716 NO₂ H CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2717 NO₂ CH₃ CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2718 NO₂ CH₂CH₃ CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2719 NO₂ (CH₂)₂CH₃ CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2720 NO₂ (CH₂)₃CH₃ CH₂CH(CH₃)-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2721 NO₂ H CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2722 NO₂ CH₃ CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2723 NO₂ CH₂CH₃ CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2724 NO₂ (CH₂)₂CH₃ CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2725 NO₂ (CH₂)₃CH₃ CH(CH₃)CH₂-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2726 NO₂ H CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2727 NO₂ CH₃ CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2728 NO₂ CH₂CH₃ CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2729 NO₂ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2730 NO₂ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2731 NO₂ H (CH₂)₂—O—C₆H₅ NCH₃ Ia1.2732 NO₂ CH₃ (CH₂)₂—O—C₆H₅ NCH₃ Ia1.2733 NO₂ CH₂CH₃ (CH₂)₂—O—C₆H₅ NCH₃ Ia1.2734 NO₂ (CH₂)₂CH₃ (CH₂)₂—O—C₆H₅ NCH₃ Ia1.2735 NO₂ (CH₂)₃CH₃ (CH₂)₂—O—C₆H₅ NCH₃ Ia1.2736 NO₂ H CH₂CH(CH₃)—O—C₆H₅ NCH₃ Ia1.2737 NO₂ CH₃ CH₂CH(CH₃)—O—C₆H₅ NCH₃ Ia1.2738 NO₂ CH₂CH₃ CH₂CH(CH₃)—O—C₆H₅ NCH₃ Ia1.2739 NO₂ (CH₂)₂CH₃ CH₂CH(CH₃)—O—C₆H₅ NCH₃ Ia1.2740 NO₂ (CH₂)₃CH₃ CH₂CH(CH₃)—O—C₆H₅ NCH₃ Ia1.2741 NO₂ H CH(CH₃)CH₂—O—C₆H₅ NCH₃ Ia1.2742 NO₂ CH₃ CH(CH₃)CH₂—O—C₆H₅ NCH₃ Ia1.2743 NO₂ CH₂CH₃ CH(CH₃)CH₂—O—C₆H₅ NCH₃ Ia1.2744 NO₂ (CH₂)₂CH₃ CH(CH₃)CH₂—O—C₆H₅ NCH₃ Ia1.2745 NO₂ (CH₂)₃CH₃ CH(CH₃)CH₂—O—C₆H₅ NCH₃ Ia1.2746 NO₂ H CH(CH₃)CH(CH₃)—O—C₆H₅ NCH₃ Ia1.2747 NO₂ CH₃ CH(CH₃)CH(CH₃)—O—C₆H₅ NCH₃ Ia1.2748 NO₂ CH₂CH₃ CH(CH₃)CH(CH₃)—O—C₆H₅ NCH₃ Ia1.2749 NO₂ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)—O—C₆H₅ NCH₃ Ia1.2750 NO₂ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)—O—C₆H₅ NCH₃ Ia1.2751 NO₂ H (CH₂)₂—O-(4-Cl—C₆H₄) NCH₃ Ia1.2752 NO₂ CH₃ (CH₂)₂—O-(4-Cl—C₆H₄) NCH₃ Ia1.2753 NO₂ CH₂CH₃ (CH₂)₂—O-(4-Cl—C₆H₄) NCH₃ Ia1.2754 NO₂ (CH₂)₂CH₃ (CH₂)₂—O-(4-Cl—C₆H₄) NCH₃ Ia1.2755 NO₂ (CH₂)₃CH₃ (CH₂)₂—O-(4-Cl—C₆H₄) NCH₃ Ia1.2756 NO₂ H CH₂CH(CH₃)—O-(4-Cl—C₆H₄) NCH₃ Ia1.2757 NO₂ CH₃ CH₂CH(CH₃)—O-(4-Cl—C₆H₄) NCH₃ Ia1.2758 NO₂ CH₂CH₃ CH₂CH(CH₃)—O-(4-Cl—C₆H₄) NCH₃ Ia1.2759 NO₂ (CH₂)₂CH₃ CH₂CH(CH₃)—O-(4-Cl—C₆H₄) NCH₃ Ia1.2760 NO₂ (CH₂)₃CH₃ CH₂CH(CH₃)—O-(4-Cl—C₆H₄) NCH₃ Ia1.2761 NO₂ H CH(CH₃)CH₂—O-(4-Cl—C₆H₄) NCH₃ Ia1.2762 NO₂ CH₃ CH(CH₃)CH₂—O-(4-Cl—C₆H₄) NCH₃ Ia1.2763 NO₂ CH₂CH₃ CH(CH₃)CH₂—O-(4-Cl—C₆H₄) NCH₃ Ia1.2764 NO₂ (CH₂)₂CH₃ CH(CH₃)CH₂—O-(4-Cl—C₆H₄) NCH₃ Ia1.2765 NO₂ (CH₂)₃CH₃ CH(CH₃)CH₂—O-(4-Cl—C₆H₄) NCH₃ Ia1.2766 NO₂ H CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) NCH₃ Ia1.2767 NO₂ CH₃ CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) NCH₃ Ia1.2768 NO₂ CH₂CH₃ CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) NCH₃ Ia1.2769 NO₂ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) NCH₃ Ia1.2770 NO₂ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)—O-(4-Cl—C₆H₄) NCH₃ Ia1.2771 NO₂ H (CH₂)₂—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2772 NO₂ CH₃ (CH₂)₂—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2773 NO₂ CH₂CH₃ (CH₂)₂—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2774 NO₂ (CH₂)₂CH₃ (CH₂)₂—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2775 NO₂ (CH₂)₃CH₃ (CH₂)₂—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2776 NO₂ H CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2777 NO₂ CH₃ CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2778 NO₂ CH₂CH₃ CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2779 NO₂ (CH₂)₂CH₃ CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2780 NO₂ (CH₂)₃CH₃ CH₂CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2781 NO₂ H CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2782 NO₂ CH₃ CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2783 NO₂ CH₂CH₃ CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2784 NO₂ (CH₂)₂CH₃ CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2785 NO₂ (CH₂)₃CH₃ CH(CH₃)CH₂—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2786 NO₂ H CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2787 NO₂ CH₃ CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2788 NO₂ CH₂CH₃ CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2789 NO₂ (CH₂)₂CH₃ CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NCH₃ Ia1.2790 NO₂ (CH₂)₃CH₃ CH(CH₃)CH(CH₃)—O-(2,4-Cl₂—C₆H₃) NCH₃

Also most particularly most extraordinarily preferred are the 2-benzoylcyclohexane-1,3-diones of the formula I which follow:

The compounds Ia2, especially the compounds Ia2.1-Ia2.2790, which differ from the corresponding compounds Ia1.1-Ia1.2790 by the fact that R¹³ is methyl:

The compounds Ia3, especially the compounds Ia3.1-Ia3.2790, which differ from the corresponding compounds Ia1.1-Ia1.2790 by the fact that R¹³ and R¹⁴ are in each case methyl:

The compounds Ia4, especially the compounds Ia4.1-Ia4.2790, which differ from the corresponding compounds Ia1.1-Ia1.2790 by the fact that R¹⁵ and R¹⁶ are in each case methyl:

The compounds Ia5, especially the compounds Ia5.1-Ia5.2790, which differ from the corresponding compounds Ia1.1-Ia1.2790 by the fact that the CR¹³R¹⁴ unit is replaced by C═O:

The compounds Ia6, especially the compounds Ia6.1-Ia6.2790, which differ from the corresponding compounds Ia1.1-Ia1.2790 by the fact that R¹¹, R¹⁵ and R¹⁶ are in each case methyl and the CR¹³R¹⁴ unit is replaced by C═O:

The compounds Ia7, especially the compounds Ia7.1-Ia7.2790, which differ from the corresponding compounds Ia1.1-Ia1.2790 by the fact that R¹¹, R¹², R¹⁵ and R¹⁶ are in each case methyl and the CR¹³R¹⁴ unit is replaced by C═O:

The compounds Ia8, especially the compounds Ia8.1-Ia8.2790, which differ from the corresponding compounds Ia1.1-Ia1.2790 by the fact that R¹ is nitro:

The compounds Ia9, especially the compounds Ia9.1-Ia9.2790, which differ from the corresponding compounds Ia1.1-Ia1.2790 by the fact that R¹ is nitro and R¹³ is methyl:

The compounds Ia10, especially the compounds Ia10.1-Ia10.2790, which differ from the corresponding compounds Ia1.1-Ia1.2790 by the fact that R¹ is nitro and R¹³ and R¹⁴ are in each case methyl:

The compounds Ia11, especially the compounds Ia11.1-Ia11.2790, which differ from the corresponding compounds Ia1.1-Ia1.2790 by the fact that R¹ is nitro and R¹⁵ and R¹⁶ are in each case methyl:

The compounds Ia12, especially the compounds Ia12.1-Ia12.2790, which differ from the corresponding compounds Ia1.1-Ia1.2790 by the fact that R¹ is nitro and the CR¹³R¹⁴ unit is replaced by C═O:

The compounds Ia13, especially the compounds Ia13.1-Ia13.2790, which differ from the corresponding compounds Ia1.1-Ia1.2790 by the fact that R¹ is nitro, R¹¹, R¹⁵ and R¹⁶ are in each case methyl and the CR¹³R¹⁴ unit is replaced by C═O:

The compounds Ia14, especially the compounds Ia14.1-Ia14.2790, which differ from the corresponding compounds Ia1.1-Ia1.2790 by the fact that R¹ is nitro, R¹¹, R¹², R¹⁵ and R¹⁶ are in each case methyl and the CR¹³R¹⁴ unit is replaced by C═O:

The compounds Ia15, especially the compounds Ia15.1-Ia15.2790, which differ from the corresponding compounds Ia1.1-Ia1.2790 by the fact that R¹ is methylsulfonyl:

The compounds Ia16, especially the compounds Ia16.1-Ia16.2790, which differ from the corresponding compounds Ia1.1-Ia1.2790 by the fact that R¹ is methylsulfonyl and R¹³ is methyl:

The compounds Ia17, especially the compounds Ia17.1-Ia17.2790, which differ from the corresponding compounds Ia1.1-Ia1.2790 by the fact that R¹ is methylsulfonyl and R¹³ and R¹⁴ are in each case methyl:

The compounds Ia18, especially the compounds Ia18.1-Ia18.2790, which differ from the corresponding compounds Ia1.1-Ia1.2790 by the fact that R¹ is methylsulfonyl and R¹⁵ and R¹⁶ are in each case methyl:

The compounds Ia19, especially the compounds Ia19.1-Ia19.2790, which differ from the corresponding compounds Ia1.1-Ia1.2790 by the fact that R¹ is methylsulfonyl and the CR¹³R¹⁴ unit is replaced by C═O:

The compounds Ia20, especially the compounds Ia20.1-Ia20.2790, which differ from the corresponding compounds Ia1.1-Ia1.2790 by the fact that R¹ is methylsulfonyl, R¹¹, R¹⁵ and R¹⁶ are in each case methyl and the CR¹³R¹⁴ unit is replaced by C═O:

The compounds Ia21, especially the compounds Ia21.1-Ia21.2790, which differ from the corresponding compounds Ia1.1-Ia1.2790 by the fact that R¹ is methylsulfonyl, R¹¹, R¹², R¹⁵ and R¹⁶ are in each case methyl and the CR¹³R¹⁴ unit is replaced by C═O:

The compounds Ia22, especially the compounds Ia22.1-Ia22.2790, which differ from the corresponding compounds Ia1.1-Ia1.2790 by the fact that R¹ is trifluoromethyl:

The compounds Ia23, especially the compounds Ia23.1-Ia23.2790, which differ from the corresponding compounds Ia1.1-Ia1.2790 by the fact that R¹ is trifluoromethyl and R¹³ is methyl:

The compounds Ia24, especially the compounds Ia24.1-Ia24.2790, which differ from the corresponding compounds Ia1.1-Ia1.2790 by the fact that R¹ is trifluoromethyl and R¹³ and R¹⁴ are in each case methyl:

The compounds Ia25, especially the compounds Ia25.1-Ia25.2790, which differ from the corresponding compounds Ia1.1-Ia1.2790 by the fact that R¹ is trifluoromethyl and R¹⁵ and R¹⁶ are in each case methyl:

The compounds Ia26, especially the compounds Ia26.1-Ia26.2790, which differ from the corresponding compounds Ia1.1-Ia1.2790 by the fact that R¹ is trifluoromethyl and the CR¹³R¹⁴ unit is replaced by C═O:

The compounds Ia27, especially the compounds Ia27.1-Ia27.2790, which differ from the corresponding compounds Ia1.1-Ia1.2790 by the fact that R¹ is trifluoromethyl, R¹¹, R¹⁵ and R¹⁶ are in each case methyl and the CR¹³R¹⁴ unit is replaced by C═O:

The compounds Ia28, especially the compounds Ia28.1-Ia28.2790, which differ from the corresponding compounds Ia1.1-Ia1.2790 by the fact that R¹ is trifluoromethyl, R¹¹, R¹², R¹⁵ and R¹⁶ are in each case methyl and the CR¹³R¹⁴ unit is replaced by C═O:

Very most particularly extraordinarily preferred compounds are the compounds of the formula Ia′ ({circumflex over (=)} I, where R¹ is bonded in position 4 of the phenyl ring and R² is bonded in position 2 of the phenyl ring)

where the variables have the following meanings:

R¹ is halogen or C₁-C₄-alkylsulfonyl;

R² is halogen or C₁-C₄-alkyl;

R³ is hydrogen or C₁-C₄-alkyl;

R⁴ is hydrogen, C₁-C₆-alkyl, C₃-C₆-alkenyl, it being possible for the two last-mentioned substituents to be partially or fully halogenated and/or to have attached to them one to three of the following groups: phenyl, phenyl-C₁-C₄-alkyl, hetaryl or phenyloxy, it being possible for the 4 last-mentioned radicals in turn to be partially or fully halogenated;

X is oxygen;

Z is oxygen or NH;

m is 0 or 1;

R₁₂ R¹², R¹⁴, R¹⁵, R¹⁶ are hydrogen or C₁-C₄-alkyl;

R¹³ is hydrogen, C₁-C₄-alkyl, tetrahydropyran-3-yl, tetrahydrothiopyran-3-yl or 1,4-dioxan-2-yl;

If desired, the CR¹³R¹⁴ unit can be replaced by C═O.

The 2-benzoylcyclohexane-1,3-diones of the formula I are obtainable by various routes, for example by the following process:

Reaction of cyclohexanediones of the formula II with an activated carboxylic acid IIIα or a carboxylic acid IIIβ which is preferably activated in situ, to give the acylation product IV, followed by a rearrangement reaction.

L¹ is a nucleophilically displaceable leaving group such as halogen, eg. bromine, chlorine, hetaryl, eg. imidazolyl, pyridyl, carboxylate, eg. acetate, trifluoroacetate and the like.

The activated carboxylic acid can be employed directly, as in the case of the carboxylic acid halides, or generated in situ, for example with dicyclohexylcarbodiimide, triphenylphosphine/azodicarboxylic ester, 2-pyridine disulfite/triphenylphosphine, carbonyldiimidazole and the like.

It may be advantageous to carry out the acylation reaction in the presence of a base. The reactants and the auxiliary base are expediently employed in equimolar amounts for this purpose. A small excess mount of the auxiliary base, for example 1.2 to 1.5 mol equivalents based on II, may be advantageous under certain circumstances.

Suitable auxiliary bases are tertiary alkylamines, pyridine or alkali metal carbonates. Examples of solvents which can be used are chlorinated hydrocarbons such as methylene chloride, 1,2-dichloroethane, aromatic hydrocarbons such as toluene, xylene, chlorobenzene, ethers such as diethyl ether, methyl tert-butyl ether, tetrahydrofuran, dioxane, polar aprotic solvents such as acetonitrile, dimethylformamide, dimethyl sulfoxide or esters such as ethyl acetate, or mixtures of these.

If carboxylic acid halides are employed as activated carboxylic acid component, it may be expedient to cool the reaction mixture to 0-10° C. when adding this reactant. The mixture is subsequently stirred at 20-100° C., preferably at 25-500° C., until the reaction is complete. Working-up is carried out in the customary manner, for example the reaction mixture is poured into water and the product of value is extracted. Solvents which are especially suitable for this purpose are methylene chloride, diethyl ether and ethyl acetate. After the organic phase has been dried and the solvent removed, the crude enol ester of the formula IV is purified, preferably by chromatography. However, it is also possible to employ the crude enol ester of the formula IV in the rearrangement reaction without further purification.

The enol esters of the formula IV are expediently subjected to a rearrangement reaction to give the compounds of the formula I at from 20 to 40° C. in a solvent and in the presence of an auxiliary base and with the aid of, or without, a cyano compound as catalyst.

Solvents which can be used are, for example, acetonitrile, ethylene chloride, 1,2-dichloroethane, ethyl acetate, toluene, or mixtures of these. The preferred solvent is acetonitrile.

Suitable auxiliary bases are tertiary amines such as triethylamine, pyridine or alkali metal carbonates such as sodium carbonate, potassium carbonate, which are preferably employed in quimolar amounts or up to a fourfold excess, based on the enol ester. By preference, triethylamine is used, preferably in twice the equimolar ratio based on the enol ester.

Suitable as “rearrangement catalysts” are inorganic cyanides such as sodium cyanide, potassium cyanide, and organic cyano compounds such as acetone cyanohydrin, trimethylsilyl cyanide. They are normally employed in an amount of from 1 to 50 mol percent, based on the enol ester. It is preferred to employ acetone cyanohydrin or trimethylsilyl cyanide, for example in an amount of from 5 to 15, preferably 10, mol percent based on the enol ester.

Work-up can be carried out in a manner known per se. For example, the reaction mixture is acidified with dilute mineral acid, eg. 5% strength hydrochloric acid or sulfuric acid, and extracted with an organic solvent, eg. methylene chloride, ethyl acetate. The organic extract can be extracted with 5-10% strength alkali metal carbonate solution, eg. sodium carbonate solution, potassium carbonate solution. The aqueous phase is acidified and the resulting precipitate filtered off with suction and/or extracted with methylene chloride or ethyl acetate, dried and concentrated. (Examples of the synthesis of enol esters of cyclohexane-1,3-diones and of the cyanide-catalyzed rearrangement reaction of the enol esters are mentioned, for example, in EP-A 186 118, U.S. Pat. No. 4 780 127).

Those cyclohexane-1,3-diones of the formula II which are used as starting materials and which are not already known can be prepared by processes known per se (for example EP-A 71 707, EP-A 142 741, EP-A 243 313, U.S. Pat. No. 4 249 937; WO 92/13821).

Novel benzoic acid derivatives of the formula III

are those where the variables have the following meanings:

R¹, R² are hydrogen, nitro, halogen, cyano, thiocyanato, C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₁-C₆-alkoxy-C₁-C₆-alkyl, C₂-C₆-alkenyl, C₂-C₆-alkynyl, —OR⁵, —OCOR⁶, —OSO₂R⁶, —SH, —S(O)_(n)R⁷, —SO₂OR⁵, —SO₂NR⁵R⁸, —NR⁸SO₂R⁶ or —NR⁸COR⁶;

R³ is hydrogen, C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₃-C₆-alkenyl or C₃-C₆-alkynyl;

R⁴ is hydrogen, C₁-C₆-alkyl, C₃-C₆-cycloalkyl, C₃-C₆-alkenyl, C₄-C₆-cycloalkenyl, C₃-C₆-alkynyl, —COR⁹, —CO₂R⁹, —COSR⁹ or —CONR⁸R⁹, it being possible for the abovementioned alkyl, cycloalkyl, alkenyl, cycloalkenyl and alkynyl radicals and for R⁹ of the radicals —COR⁹, —CO₂R⁹, —COSR⁹ and —CONR⁸R⁹ to be partially or fully halogenated and/or to have attached to them one to three of the following groups:

 hydroxyl, mercapto, amino, cyano, R¹⁰, —OR¹⁰, —SR¹⁰, —NR⁸R¹⁰, ═NOR¹⁰, —OCOR¹⁰, —SCOR¹⁰, —NR⁸COR¹⁰, —CO₂R¹⁰, —COSR¹⁰, —CONR⁸R¹⁰, C₁-C₄-alkyliminooxy, C₁-C₄-alkoxyamino, C₁-C₄-alkylcarbonyl, C₁-C₄-alkoxy-C₂-C₆-alkoxycarbonyl, C₁-C₄-alkylsulfonyl, heterocyclyl, heterocyclyloxy, phenyl, phenyl-C₁-C₄-alkyl, hetaryl, phenoxy, phenyl-C₁-C₄-alkoxy and hetaryloxy, it being possible for the eight last-mentioned radicals, in turn, to be substituted;

X is oxygen or sulfur;

Z is oxygen or NR⁸;

m is 0 or 1;

n is 0, 1 or 2;

R⁵ is hydrogen, C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₁-C₆-alkoxy-C₂-C₆-alkyl, C₃-C₆-alkenyl or C₃-C₆-alkynyl;

R⁶ is C₁-C₆-alkyl or C₁-C₆-haloalkyl;

R⁷ is C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₄-C₆-alkoxy-C₂-C₆-alkyl, C₃-C₆-alkenyl or C₃-C₆-alkynyl;

R⁸ is hydrogen or C₁ -C ₆-alkyl;

R⁹ is C₁-C₆-alkyl, C₃-C₆-alkenyl, C₃-C₆-alkynyl, phenyl or benzyl;

R¹⁰ is C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₃-C₆-alkenyl or C₃-C₆-alkynyl;

R¹⁷ is hydroxyl or a radical which can be removed by hydrolysis,

where m is 1 if R³ is hydrogen.

Examples of radicals which can be removed by hydrolysis are alkoxy, phenoxy, alkylthio and phenylthio radicals which are unsubstituted or substituted, halides, hetaryl radicals which are bonded via nitrogen, amino radicals, imino radicals which are unsubstituted or substituted.

Preferred are benzoic acid halides IIIα, where L¹=halogen ({circumflex over (=)} III where R¹⁷=halogen),

where the variables R¹ to R⁴, X, Z and m have the meanings given under formula III and

L¹ is halogen, in particular chlorine or bromine.

Equally preferred are the benzoic acids of the formula IIIβ ({circumflex over (=)} III where R¹⁷=hydroxyl),

where the variables R¹ to R⁴, X, Z and m have the meanings given under formula III.

Equally preferred are the benzoic esters of the formula IIIγ ({circumflex over (=)} III where M=C₁-C₆-alkoxy)

where the variables R¹ to R⁴, X, Z and m have the meanings given under formula III and

M is C₁-C₆-alkoxy;

The particular embodiments of the benzoic esters of the formula III with reference to the variables R¹ to R⁴, X, Z and M correspond to those of the 2-benzoylcyclohexane-1,3-diones of the formula I.

The compounds of the formula IIIα (where L¹ =halogen) can be synthesized by reacting benzoic acids of the formula IIIβ with halogenating reagents such as thionyl chloride, thionyl bromide, phosgene, diphosgene, triphosgene, oxalyl chloride, oxalyl bromide by methods similar to those known from the literature (cf. L. G. Fieser, M. Fieser “Reagents for Organic Synthesis”, Vol. I (1967), pp. 767-769.

The benzoic acids of the formula IIIβ can be obtained, inter alia, by hydrolyzing the benzoic esters of the formula IIIγ (where M=C₁-C₆-alkoxy) by methods similar to those known from the literature.

The benzoic esters of the formula IIIγ (where X=oxygen) are obtainable by various routes, for example by the following processes:

Isophthalic acid derivatives of the formula VI can be obtained in a manner known per se by oxidizing aldehydes of the formula V (J. March, “Advanced Organic Chemistry”, 3rd Edition (1985), p. 629 et seq., Wiley-Interscience Publication).

Methods which are similar to those known from the literature can be used for first converting the compounds of the formula VI into the corresponding activated carboxylic acids VII where L² is a nucleophilically displaceable leaving group such as halogen, eg. bromine, chlorine, hetaryl, eg. imidazolyl, pyridyl, carboxylate, eg. acetate, trifluoroacetate and the like. Then, in case a₁) the product is reacted with an amino, hydroxylamine or hydrazine derivative, where R³ is hydrogen. Subsequent alkylation (a₂) gives corresponding amide, hydroxamic acid or carbohydrazide derivatives of the formula IIIγ (where X=0 and R³≠H) (where L³ has the meaning given under L²) (J. Org. Chem. (1971), 31, 284-294; J. Chem. Soc. Perk. II (1977), 1080-1084; Australian J. Chem. (1969), 22, 161-173; ibid (1974), 27, 1341-1349). In case b), the end product is obtained by direct reaction with R³NH—(Z)_(m)—R⁴ (cf. Australian J. Chem. (1974), 27, 1341-1349).

The aldehydes of the formula V can be synthesized from the corresponding toluenes of the formula VIII by processes similar to those known from the literature by converting them into the ω-halotoluene IX and subsequently oxidizing the product (cf. Synth. Commun. 22 (1992), 1967-1971).

The carboxylic acids of the formula VI are accessible by hydrolyzing nitriles of the formula X by processes known from the literature (J. March, “Advanced Organic Chemistry”, 3rd Edition (1970), p. 788, Wiley-Interscience Publication, 1985; Ann. Chem. (1970), p. 23-37).

The nitrites of the formula X can be synthesized from the corresponding aldehydes V by processes similar to those known from the literature (J. March, “Advanced Organic Chemistry”, 3rd Edition (1985), pp. 806-807, Wiley-Interscience Publication). Equally, it is possible to obtain nitrites of the formula X from anilines of the formula XI by means of Sandmeyer reaction or from aryl halides of the formula XII by Rosemund/von Braun reaction with metal cyanides, in particular CUCN (J. March, “Advanced Organic Chemistry”, 1985, 3rd Edition, p. 594, p. 648, Wiley-Interscience Publication).

Preparation Examples 2-[2,4-Dichloro-3-(N-ethyl-N-propoxyaminocarbonyl)benzoyl]-1,3-cyclohexanedione (compound 2.03)

2.20 g (0.0065 mol) of 2,4-dichloro-3-(N-ethyl-N-propoxyaminocarbonyl)benzoyl chloride were added to a solution of 0.71 g (0.0070 mol) of triethylamine and 0.79 g (0.0070 mol) of 1,3-cyclohexanedione in 50 ml of methylene chloride. After the reaction solution had been stirred for 2 hours at room temperature, the solvent was removed in vacuo. The residue was purified by means of silica gel chromatography (eluent: toluene/ethyl acetate=8/2). The resulting enol ester was taken up in 50 ml of acetonitrile, and 0.50 g (0.0049 mol) of triethylamine and 0.10 g (0.0010 mol) of trimethylsilyl cyanide were added. After the mixture had been stirred for 3 hours at room temperature, the solvent was removed and the residue was taken up in methylene chloride. The organic phase was washed with dilute phosphoric acid, dried and concentrated. This gave 1.20 g of 2-[2,4-dichloro-3-(N-ethyl-N-propoxyaminocarbonyl)benzoyl]-1,3-cyclohexanedione, which was extracted by stirring with diethyl ether.

(m.p.: 180-183° C.)

Besides the 2-benzoylcyclohexane-1,3-dione of the formula I described above, other substances which were, or can be, prepared in a similar manner are listed in Table 2 which follows:

TABLE 2 Ia

Physical data m.p. No. Z R¹ R² R³ R⁴ R¹¹ R¹² R¹³ R¹⁴ R¹⁵ R¹⁶ [° C.] 2.01  O Cl Cl CH₃ CH₃ H H H H H H 127-128 2.02  O Cl Cl CH₃ CH₂-(4-Cl—C₆H₄) H H H H H H 182-183 2.03  O Cl Cl CH₂CH₃ (CH₂)₂CH₃ H H H H H H 182-183 2.04  O Cl Cl CH₃ (CH₂)₂CH₃ H H H H H H 177-178 2.05  O Cl Cl CH₃ CH₂-(4-Cl—C₆H₄) H H

H H H >200 2.06  O Cl Cl CH₃ CH₂-(4-Cl—C₆H₄) CH₃ CH₃ ═O CH₃ CH₃ 185-200 2.07  O Cl Cl CH₃ CH₂-(4-Cl—C₆H₄) H H

H H H 165-187 2.08  O Cl Cl CH₃ (CH₂)₂CH₃ H H

H H H 50-55 2.09  O Cl Cl CH₃

H H H H H H 159-166 2.10 O Cl Cl CH₃

H H H H H H 60-67 2.11 O Cl Cl CH₃

H H

H H H 157-163 2.12 O SO₂CH₃ Cl CH₃ CH₃ CH₃ CH₃ ═O CH₃ CH₃ 190-210 2.13 O SO₂CH₃ Cl CH₃ CH₃ H H H H H H >200 2.14 O SO₂CH₃ Cl CH₃ CH₃ H H H H CH₃ CH₃ >200 2.15 O SO₂CH₃ Cl CH₃ CH₃ H H CH₃ CH₃ H H >200 2.16 O SO₂CH₃ Cl CH₂CH₃ CH₃ H H H H H H 160-175 2.17 O SO₂CH₃ Cl CH₂CH₃ CH₂CH₃ H H H H H H 72-80 2.18 O SO₂CH₃ Cl CH₃ CH₂CH₃ H H H H H H  75-113 2.19 O SO₂CH₃ Cl H (E)-CH₂CH═CHCl H H H H H H 177-180 2.20 O SO₂CH₃ Cl CH₃ (E)-CH₂CH═CHCl H H H H H H 195-197 2.21 NH SO₂CH₃ Cl CH₃ H H H H H H H 168-178 2.22 — SO₂CH₃ Cl CH₃ CH₃ H H H H H H 200-201 2.23 — SO₂CH₃ Cl CH₃ CH₃ H H CH₃ CH₃ H H 160-162 2.24 — SO₂CH₃ Cl CH₃ CH₃ H H H H CH₃ CH₃ 194-197 2.25 — SO₂CH₃ CH₃ CH₃ CH₃ CH₃ CH₃ ═O CH₃ CH₃  75-130 2.26 — SO₂CH₃ CH₃ CH₃ CH₃ H H CH₃ CH₃ H H 170-181 2.27 — Cl Cl CH₃ CH₂CH₃ H H H H H H 193-198 2.28 O SO₂CH₃ Cl CH₂CH₃ CH₃ H H CH₃ CH₃ H H 154-155 2.29 O SO₂CH₃ Cl H CH₃ H H H H H H 164-168 2.30 — SO₂CH₃ Cl (CH₂)₂CH₃ H H H H H H H 164-168 2.31 — SO₂CH₃ Cl CH₃ H H H H H H H 180-183 2.32 — SO₂CH₃ Cl CH₃ H CH₃ CH₃ H H H H >200

The syntheses of some starting materials are given below: Methyl 2-chloro-3-(N-ethoxy-N-methylaminocarbonyl)-4-methylsulfonylbenzoate (compound 3.29)

Step a) 2-Chloro-3-methyl-4-methylthioacetophenone

A solution of 157 g (2 mol) of acetyl chloride in 420 mol of 1,2-dichloroethane was added dropwise at 15-20° C. to a suspension of 286 g (2.14 mol) of aluminum trichloride in 420 ml of 1,2-dichloroethane. A solution of 346 g (2 mol) of 2-chloro-6-methylthiotoluene in 1 l of 1,2-dichloroethane was subsequently added dropwise. After the reaction mixture had been stirred for 12 hours, it was poured into a mixture of 3 l of ice and 1 l of concentrated HCl. The mixture was extracted with methylene chloride, and the organic phase was washed with water, dried with sodium sulfate and concentrated. The residue was distilled in vacuo. This gave 256 g (60% of theory) of 2-chloro-3-methyl-4-methylthioacetophenone.

(m.p.: 460° C. )

Step b) 2-Chloro-3-methyl-4-methylsulfonylacetophenone

163.0 g (0.76 mol) of 2-chloro-3-methyl-4-methylthio-acetophenone were dissolved in 1.5 1 of glacial acetic acid, 18.6 g of sodium tungstate were added, and 173.3 g of 30% strength hydrogen peroxide solution were added dropwise with cooling. Stirring was continued for 2 days and the mixture was subsequently diluted with water. The solid which had precipitated was filtered off with suction, washed with water and dried. This gave 164.0 g (88% of theory) of 2-chloro-3-methyl-4-methyl-sulfonylacetophenone.

(m.p.: 110-111° C.)

Step c) 2-Chloro-3-methyl-4-methylsulfonylbenzoic acid 82 g (0.33 mol) of 2-chloro-3-methyl-4-methylsulfonyl-acetophenone were dissolved in 700 ml of dioxane, and 1 l of a 12.5% strength sodium hypochlorite solution was added at room temperature. Stirring was subsequently continued for 1 hour at 800° C. After cooling, two phases formed, of which the bottom phase was diluted with water and acidified weakly. The solid which precipitated was filtered off with suction, washed with water and dried. This gave 60 g (73% of theory) of 2-chloro-3-methyl-4-methylsulfonylbenzoic acid.

(m.p.: 230-231° C.)

Step d) Methyl 2-chloro-3-methyl-4-methylsulfonylbenzoate

100 g (0.4 mol) of 2-chloro-3-methyl-4-methyl-sulfonylbenzoic acid were dissolved in 1 l of methanol and hydrogen chloride gas was passed in for 5 hours at reflux temperature. The mixture was subsequently concentrated. This gave 88.5 g (84% of theory) of methyl 2-chloro-3-methyl-4-methylsulfonylbenzoate.

(m.p.: 107-108° C.)

Step e) Methyl 3-bromomethyl-2-chloro-4-methylsulfonylbenzoate

82 g (0.31 mol) of methyl 2-chloro-3-methyl-4-methyl-sulfonylbenzoate were dissolved in 2 1 of tetrachloromethane, 56 g (0.31 mol) of N-bromosuccinimide were added, a little at a time, with exposure to light. The reaction mixture was filtered, the filtrate was concentrated, and the residue was taken up in 200 ml of methyl tert-butyl ether. The solution was treated with petroleum ether, and the solid which precipitated was filtered off with suction and dried. This gave 74.5 g (70% of theory) of methyl 3-bromomethyl-2-chloro-4-methylsulfonylbenzoate.

(m.p.: 74-75° C.)

Step f) Methyl 2-chloro-3-formyl-4-methylsulfonylbenzoate

42.1 g (0.36 mol) of N-methylmorpholine-N-oxide were added to a solution of 41.0 g (0.12 mol) of methyl 3-bromomethyl-2-chloro-4-methylsulfonylbenzoate in 250 ml of acetonitrile. The batch was stirred for 12 hours at room temperature and subsequently concentrated, and the residue was taken up in ethyl acetate. The solution was extracted with water, dried with sodium sulfate and concentrated. This gave 31.2 g (94% of theory) of methyl 2-chloro-3-formyl-4-methylsulfonylbenzoate

(m.p.: 98-105° C.)

Step g) Methyl 2-chloro-3-hydroxycarbonyl-4-methylsulfonylbenzoate

13.8 g (0.11 mol) of sodium hydrogen phosphate monohydrate in 170 ml of water, 49.3 g (0.43 mol) of 30% strength hydrogen peroxide solution and 66.2 g (0.59 mol) of 80% strength aqueous sodium chlorite solution were added in succession at 5° C. to a solution of 115.3 g (0.42 mol) of methyl 2-chloro-3-formyl-4-methyl-sulfonylbenzoate and in 2000 ml of acetonitrile. The reaction solution was stirred for 1 hour at 5° C. and for 12 hours at room temperature. Then, the pH was brought to 1 with 10% strength hydrochloric acid, and 1500 ml of aqueous 40% strength sodium hydrogen sulfite solution were added. After the mixture had been stirred for 1 hour at room temperature, the aqueous phase was extracted three times with ethyl acetate. The combined organic phases were washed with sodium hydrogen sulfite solution and dried. After the solvent had been distilled off, 102.0 g of methyl 2-chloro-3-hydroxycarbonyl-4-methylsulfonylbenzoate were obtained.

(¹H NMR (d⁶-DMSO, δ in ppm): 3.34 (s, 3H); 3.93 (s, 3H); 8.08 (s, 2H); 14.50 (s, br., 1H))

Step h) Methyl 2-chloro-3-chlorocarbonyl-4-methylsulfonylbenzoate

2 drops of dimethylformamide and 11.9 g (0.1 mol) of thionyl chloride were added to a solution of 6.0 g (0.021 mol) of methyl 2-chloro-3-hydroxycarbonyl-4-methylsulfonylbenzoate and in 50 ml of dry toluene. The solution was refluxed for 4 hours. After the solvent had been removed in vacuo, 6.2 g of methyl 2-chloro-3-chlorocarbonyl-4-methylsulfonylbenzoate were obtained.

(¹H NMR (CDCl₃; δ in ppm): 3.21 (s, 3H); 4.02 (s, 3H); 8.02 (d, 1H); 8.07 (d, 1H))

Step i) Methyl 2-chloro-3-N-ethoxyaminocarbonyl-4-methylsulfonylbenzoate (compound 3.28)

11.70 g (0.120 mol) of O-ethyl hydroxylamine hydrochloride and 12.10 g (0.120 mol) of triethylamine were added at room temperarture to a solution of 26.40 g (0.085 mol) of methyl 2-chloro-3-chlorocarbonyl-4-methylsulfonylbenzoate and in 300 ml of dichloromethane. After the reaction solution had been stirred for 4 hours at room temperature, it was washed with dilute hydrochloric acid, dried and concentrated. The resulting residue was extracted by stirring with diethyl ether. This gave 25.00 g of methyl 2-chloro-3-N-ethoxyaminocarbonyl-4-methylsulfonyl-benzoate.

(m.p.: 90-110° C.)

Step j) Methyl 2-chloro-3-(N-ethoxy-N-methylaminocarbonyl)-4-methylsulfonylbenzoate (compound 3.29)

A mixture of 20.00 g (0.060 mol) of methyl 2-chloro-3-N-ethoxyaminocarbonyl-4-methylsulfonylbenzoate and 16.60 g (0.120 mol) of potassium carbonate in 200 ml of dimethylformamide was stirred for 30 minutes at room temperature. 25.60 g (0.180 mol) of methyl iodide were subsequently added dropwise, and the mixture was stirred for 5 hours at 50° C. After the reaction mixture had cooled, it was stirred into 1 l of ice-water, the aqueous phase was extracted with ethyl acetate, and the combined organic phases were dried and concentrated. The residue was chromatographed on silica gel (eluent: toluene/ethyl acetate=8/2). This gave 3.80 g of methyl 2-chloro-3-(N-ethoxy-N-methylaminocarbonyl)-4-methyl-sulfonylbenzoate.

2,4-Dichloro-3-(N-ethyl-N-propoxy)aminocarbonylbenzoyl chloride (compound 3.21)

Step a) 2,4-Dichloro-3-methylacetophenone

235.0 g (3.0 mol) of acetyl chloride were added dropwise in the course of 2 hours to a solution of 502.0 g (3.12 mol) of 2,6-dichlorotoluene and [sic] 408.0 g (3.06 mol) of aluminum trichloride at 100° C. , with stirring. After the reaction mixture had been stirred for 2 hours at 100-105° C., it was cooled and poured onto 3 l of ice and 1 l of water. The solid which precipitated in this process was filtered off with suction and washed to neutrality with 800 ml of water. After drying at 40° C., 500.0 g of 2,4-dichloro-3-methylacetophenone were obtained as crude product, which was subsequently distilled under a high vacuum.

(b.p.: 121-128° C. (4 mbar))

step b) 2,4-Dichloro-3-methylbenzoic acid

Firstly 655.2 g (4.1 mol) of bromine and subsequently 203.0 g (1.0 mol) of 2,4-dichloro-3-methylacetophenone in 1300 ml of 1,4-dioxane were added dropwise at 0-10° C. to a solution of 520.0 g (13 mol) of sodium hydroxide in 2600 ml of water. After the mixture had been stirred for 12 hours, the organic phase was separated off, the aqueous phase was treated with a 30% strength solution made with sodium pyrosulfite and water, and the pH was brought to 1 with hydrochloric acid. The precipitate which had separated out was filtered off with suction, washed with water and dried in vacuo at 60° C. This gave 197.0 g of 2,4-dichloro-3-methylbenzoic acid.

(m.p.: 173-175° C.)

Step c) Methyl 2,4-dichloro-3-methylbenzoate

60 ml of concentrated sulfuric acid were added dropwise to a solution of 424.0 g (2 mol) of 2,4-dichloro-3-methylbenzoic acid and in 1500 ml of methanol. After the reaction mixture had been refluxed for 5 hours, it was cooled and concentrated in vacuo, and the residue was subsequently taken up in 1000 ml of methylene chloride. The organic phase was washed with water, subsequently with 5% strength sodium hydrogen carbonate solution and then again with water, dried and concentrated in vacuo. This gave 401.0 g of methyl 2,4-dichloro-3-methylbenzoate.

(b.p: 103-107° C. (1-1.5 mbar))

Step d) Methyl 3-bromomethyl-2,4-dichlorobenzoate

1.0 g of azobisisobutyronitrile was added to a solution of 84.0 g (0.38 mol) of methyl 2,4-dichloro-3-methylbenzoate and 67.6 g (0.38 mol) of N-bromosuccinimide in 380 ml of carbon tetrachloride. After the reaction mixture had been refluxed for 3.5 hours, it was cooled, and the precipitate formed was filtered off with suction. The filtrate was concentrated in vacuo and the resulting residue was extracted by stirring with methyl tert-butyl ether. This gave 108.0 g of methyl 3-bromomethyl-2,4-dichlorobenzoate.

(m.p.: 51-54° C.)

Step e) Methyl 2,4-dichloro-3-formylbenzoate

696.2 g (2.97 mol) of aqueous 50% strength N-methylmorpholine N-oxide solution were added dropwise under reflux to a solution of 312.0 g (0.99 mol) of methyl 3-bromomethyl-2,4-dichlorobenzoate in 2 l of acetonitrile. After the reaction solution had been stirred for 48 hours at room temperature, it was stirred into 6 l of water. The precipitate which had separated out was filtered off with suction, washed with water and dried in vacuo. This gave 141.3 g of methyl 2,4-dichloro-3-formylbenzoate.

(¹H NMR (CDCl₃, δ in ppm): 3.98 (s, 3H); 7.47 (d, 1H); 7.84 (d, 1H); 10.48 (s, 1H))

Step f) Methyl 2,4-dichloro-3-hydroxycarbonylbenzoate

5.9 g (0.043 mol) of sodium dihydrogen phosphate monohydrate in 70 ml of water, 20.5 g (0.181 mol) of 30% strength hydrogen peroxide solution and 27.3 g (0.241 mol) of 80% strength sodium chlorite solution were added in succession at 5° C. to a solution of 40.0 g (0.172 mol) of methyl 2,4-dichloro-3-formylbenzoate and in 500 ml of acetonitrile. The reaction solution was stirred for 1 hour at 5° C. and for 12 hours at room temperature. Subsequently, a pH of 1 was established with 10% strength hydrochloric acid, and 500 ml of 40% strength sodium hydrogen sulfite solution were added. After the mixture had been stirred for 1 hour at room temperature, the aqueous phase was extracted three times with ethyl acetate, the combined organic phases were washed with 1.0 l of 10% strength sodium hydrogen sulfite solution and subsequently dried. After the solvent had been distilled off, 40.0 g of methyl 2,4-dichloro-3-hydroxycarbonylbenzoate were obtained.

(¹H NMR (d⁶-DMSO, δ in ppm): 3.90 (s, 3H); 7.69 (d, 1H); 7.89 (d, 1H))

Step g) Methyl 3-chlorocarbonyl-2,4-dichlorobenzoate 2 drops of dimethylformamide and 11.90 g (0.1 mol) of thionyl chloride were added to a solution of 5.00 g (0.02 mol) of methyl 2,4-dichloro-3-hydroxycarbonyl-benzoate and in 50 ml of dry toluene. The solution was refluxed for 4 hours. After the solvent had been distilled off, 5.35 g of methyl 3-chlorocarbonyl-2,4-dichlorobenzoate were obtained.

Step h) Methyl 2,4-dichloro-3-(N-propoxy)aminocarbonylbenzoate (compound 3.17)

4.05 g (0.040 mol) of triethylamine and 4.50 g (0.040 mol) of propoxyamine hydrochloride were added to a solution of 10.70 g (0.040 mol) of methyl 3-chlorocarbonyl-2,4-dichlorobenzoate and [sic] 200 ml of dichloromethane. After the reaction solution had been stirred for 2 hours at room temperature, it was washed with dilute phosphoric acid, dried and concentrated. The residue obtained was chromatographed on silica gel (eluent: toluene/ethyl acetate=9/1). This gave methyl 2,4-dichloro-3-(N-propoxy)aminocarbonylbenzoate.

Step i) Methyl 2,4-dichloro-3-(N-ethyl-N-propoxy)-aminocarbonylbenzoate (compound 3.14)

A mixture of 12.50 g (0.041 mol) of methyl 2,4-dichloro-3-(N-propoxy)aminocarbonylbenzoate and 11.30 g (0.082 mol) of potassium carbonate in 100 ml of dimethylformamide was stirred for 30 minutes at room temperature. 19.20 g (0.123 mol) of ethyl iodide were subsequently added dropwise. After the reaction mixture had been heated for 5 hours at 50° C., it was cooled and stirred into 1 l of ice-water. The aqueous phase was then extracted with ethyl acetate, the combined organic phases were dried, and the solvent was distilled off in vacuo. After the residue had been chromatographed on silica gel (eluent: toluene/ethyl acetate=9/1), 7.00 g of methyl 2,4-dichloro-3-(N-ethyl-N-propoxy)aminocarbonylbenzoate were obtained.

(m.p.: 48-50° C.).

Step j) 2,4-Dichloro-3-(N-ethyl-N-propoxy)aminocarbonylbenzoic acid (compound 3.18)

A solution of 7.00 g (0.021 mol) of methyl 2,4-dichloro-3-(N-ethyl-N-propoxy)aminocarbonylbenzoate and [sic] 40 ml of 10% strength aqueous sodium hydroxide solution was stirred for 2 hours at 80° C. After the reaction mixture had cooled, it was stirred into 200 ml of ice-water, and the pH was brought to 1 with concentrated hydrochloric acid. The aqueous phase was extracted with ethyl acetate, and the combined organic phases were dried and concentrated in vacuo. This gave 5.50 g of 2,4-dichloro-3-(N-ethyl-N-propoxy)-aminocarbonylbenzoic acid.

Step k) 2,4-Dichloro-3-(N-ethyl-N-propoxy)aminocarbonylbenzoyl chloride (compound 3.21)

A solution of 4.00 g (0.0125 mol) of 2,4-dichloro-3-(N-ethyl-N-propoxy)aminocarbonylbenzoic acid and 14.90 g of thionyl chloride in 100 ml of dry toluene was stirred for 3 hours at 100° C. After the solvent had been removed in vacuo, 4.40 g of 2,4-dichloro-3-(N-ethyl-N-propoxy)-aminocarbonylbenzoyl chloride were obtained.

Methyl 2,4-dichloro-3-(N-methoxy)aminocarbonylbenzoate (compound 3.01)

20 4.60 g (0.045 mol) of triethylamine and 3.75 g (0.045 mol) of methoxyamine hydrochloride were added to a solution of 5.35 g (0.02 mol) of methyl 3-chlorocarbonyl-2,4-dichlorobenzoate and in 100 ml of dichloromethane. After the reaction solution had been stirred for 12 hours at room temperature, it was washed with dilute phosphoric acid, dried and concentrated. The resulting residue was extracted by stirring with diethyl ether. This gave 4.80 g of methyl 2,4-dichloro-3-(N-methoxy)aminocarbonylbenzoate.

(m.p.: 162-164° C.)

30 Methyl 2,4-dichloro-3-(N-propoxy)aminocarbonylbenzoate (compound 3.02)

10.7 g (0.04 mol) of methyl 3-chlorocarbonyl-2,4-dichlorobenzoate in 100 ml of methylene chloride were slowly added dropwise at 30° C. to a solution of 4.50 g (0.04 mol) of propoxyamine hydrochloride and 4.05 g (0.04 mol) of triethylamine in 200 ml of methylene chloride. After the reaction mixture had been stirred for 2 hours at room temperature, it was washed with dilute phosphoric acid, dried and concentrated. The resulting residue was chromatographed on silica gel (eluent: toluene/ethyl acetate=9/1). This gave 11.50 g of methyl 2,4-dichloro-3-(N-propoxyamino)carbonylbenzoate.

(m.p.: 80-81° C.)

Methyl 3-(N-4-chlorobenzyloxy)aminocarbonyl-2,4-dichlorobenzoate (compound 3.03)

10.70 g (0.04 mol) of methyl 3-chlorocarbonyl-2,4-dichloro-benzoate in 50 ml of methylene chloride were slowly added dropwise at approximately 30° C. to a solution of 7.76 g (0.04 mol) of 4-chlorobenzyloxyamine hydrochloride and 4.05 g (0.04 mol) of triethylamine in 200 ml of methylene chloride. After the reaction mixture had been stirred for 12 hours at room temperature, it was washed with dilute phosphoric acid, dried and concentrated. After the residue had been extracted by stirring with diethyl ether, 19.00 g of methyl 3-(4-chlorobenzyloxy)amino-carbonyl-2,4-dichlorobenzoate were obtained.

(m.p.: 120-121° C.)

Besides the compounds described above, other benzoic acid derivatives of the formula IIIa which were, or can be, prepared in a similar manner are listed in Table 3 below.

TABLE 3 IIIa

({circumflex over (=)} III where R¹ is bonded in the 4-position and R² in the 2-position) M.p. [° C.] ¹H NMR No. X R¹ R² R³ (Z)_(m)—R⁴ R¹⁷ [ppm] 3.01 O Cl Cl H OCH₃ OCH₃ 162-164 3.02 O Cl Cl H O(CH₂)₂CH₃ OCH₃ 80-81 3.03 O Cl Cl H

OCH₃ 120-121 3.04 O Cl Cl CH₃ OCH₃ OCH₃ 78-80 3.05 O Cl Cl CH₃ OCH₃ OH 3.06 S Cl Cl CH₃ OCH₃ OCH₃ 3.07 O Cl Cl CH₃ OCH₃ Cl 3.08 O Cl Cl H OCH₃ OH 3.09 O Cl Cl H OCH₃ Cl 3.10 O Cl Cl CH₃

OCH₃ 121-123 3.11 O Cl Cl CH₃ CH₂CH₃ OCH₃ 3.12 O Cl Cl CH₃ CH₂CH₃ OH 151-153 3.13 O Cl Cl CH₃ O(CH₂)₂CH₃ OCH₃ 47-48 3.14 O Cl Cl C₂H₅ O(CH₂)₂CH₃ OCH₃ 48-50 3.15 O Cl Cl CH₃

OH 130-131 3.16 O Cl Cl CH₃ O(CH₂)₂CH₃ OH oil 3.17 O Cl Cl H O(CH₂)₂CH₃ OCH₃ 80-81 3.18 O Cl Cl C₂H₅ O(CH₂)₂CH₃ OH oil 3.19 O Cl Cl CH₃ CH₂CH₃ Cl 3.20 O Cl Cl CH₃

Cl 3.21 O Cl Cl C₂H₅ O(CH₂)₂CH₃ Cl 3.22 O SO₂CH₃ Cl H OCH₃ OCH₃ 160-162 3.23 O SO₂CH₃ Cl CH₃ OCH₃ OCH₃ 102-103 3.24 O Cl Cl H N(CH₃)₂ OCH₃ 170-176 3.25 O Cl Cl H

OCH₃ 3.26 O Cl Cl CH₃

OCH₃ 3.27 O Cl Cl CH₃

OH 110-118 3.28 O SO₂CH₃ Cl H OCH₂CH₃ OCH₃  90-110 3.29 O SO₂CH₃ Cl CH₃ OCH₂CH₃ OCH₃ 3.30 O SO₂CH₃ Cl CH₃ OCH₂CH₃ OH 3.31 O SO₂CH₃ Cl CH₃ OCH₃ OH 3.32 O SO₂CH₃ Cl CH₃ OCH₃ Cl 3.33 O SO₂CH₃ Cl CH₂CH₃ OCH₃ OCH₃ 140-144 3.34 O SO₂CH₃ Cl CH₂CH₃ OCH₃ OH 194-197 3.35 O SO₂CH₃ Cl CH₃ OCH₂CH₃ OH  98-103 3.36 O SO₂CH₃ Cl CH₂CH₃ OCH₂CH₃ OCH₃ 3.37 O SO₂CH₃ Cl CH₂CH₃ OCH₂CH₃ OH 3.38 O SO₂CH₃ Cl H (E)-OCH₂CH═CHCl OH 204 3.39 O SO₂CH₃ Cl CH₃ (E)-OCH₂CH═CHCl OH 57-60 3.40 O SO₂CH₃ CH₃ CH₃ CH₃ OH 249-270 3.41 O Cl Cl CH₃ N(CH₃)₂ OCH₃  93 3.42 O SO₂CH₃ Cl C(CH₃)₂CH₂Cl H OCH₃ 147-148 3.43 O SO₂CH₃ Cl H OCH₃ OH oil 3.44 O SO₂CH₃ Cl (CH₂)₂CH₃ H OH 168-170 3.45 O SO₂CH₃ Cl CH₃ NH₂ OH 203-205 3.46 O SO₂CH₃ Cl CH₃ H NHCH₃ oil 3.47 O SO₂CH₃ Cl CH₃ H OH oil

The 2-benzoylcyclohexane-1,3-diones of the formula I and their agriculturally useful salts are suitable as herbicides, both in the form of isomer mixtures and in the form of the pure isomers. The herbicidal compositions comprising compounds of the formula I effect very good control of vegetation on non-crop areas, especially at high rates of application. In crops such as wheat, rice, maize, soybeans and cotton they act against broad-leaved weeds and grass weeds without damaging the crop plants substantially. This effect is observed especially at low rates of application.

Depending on the application method in question, the compounds of the formula I, or compositions comprising them, can additionally be employed in a further number of crop plants for eliminating undesirable plants. Examples of suitable crops are the following:

Allium cepa, Ananas comosus, Arachis hypogaea, Asparagus officinalis, Beta vulgaris spec. altissima, Beta vulgaris spec. rapa, Brassica napus var. napus, Brassica napus var. napobrassica, Brassica rapa var. silvestris, Camellia sinensis, Carthamus tinctorius, Carya illinoinensis, Citrus limon, Citrus sinensis, Coffea arabica (Coffea canephora, Coffea liberica), Cucumis sativus, Cynodon dactylon, Daucus carota, Elaeis guineensis, Fragaria vesca, Glycine max, Gossypium hirsutum, (Gossypium arboreum, Gossypium herbaceum, Gossypium vitifolium), Helianthus annuus, Hevea brasiliensis, Hordeum vulgare, Humulus lupulus, Ipomoea batatas, Juglans regia, Lens culinaris, Linum usitatissimum, Lycopersicon lycopersicum, Malus spec., Manihot esculenta, Medicago sativa, Musa spec., Nicotiana tabacum (N.rustica), Olea europaea, Oryza sativa, Phaseolus lunatus, Phaseolus vulgaris, Picea abies, Pinus spec., Pisum sativum, Prunus avium, Prunus persica, Pyrus communis, Ribes syl estre [sic], Ricinus communis, Saccharum officinarum, Secale cereale, Solanum tuberosum, Sorghum bicolor (s. vulgare), Theobroma cacao, Trifolium pratense, Triticum aestivum, Triticum durum, Vicia faba, Vitis vinifera and Zea mays.

Moreover, the compounds of the formula I can also be used in crops which tolerate the action of herbicides due to breeding including genetic engineering methods.

The compounds of the formula I or the herbicidal compositions comprising them, can be employed, for example, in the form of directly sprayable aqueous solutions, powders, suspensions, also highly-concentrated aqueous, oily or other suspensions or dispersions, emulsions, oil dispersions, pastes, dusts, materials for spreading or granules, by means of spraying, atomizing, dusting, spreading or pouring. The use forms depend on the intended purposes; in any case, they should guarantee the finest possible distribution of the active ingredients according to the invention.

The herbicidal compositions comprise a herbicidally active amount of at least one compound of the formula I or of an agriculturally useful salt of I and auxiliaries conventionally used for the formulation of crop protection products.

Suitable inert additives are essentially: mineral oil fractions of medium to high boiling point such as kerosine and diesel oil, furthermore coal tar oils and oils of vegetable or animal origin, aliphatic, cyclic and aromatic hydrocarbons, e.g. paraffin, tetrahydronaphthalene, alkylated naphthalenes and their derivatives, alkylated benzenes and their derivatives, alcohols such as methanol, ethanol, propanol, butanol, cyclohexanol, ketones such as cyclohexanone, and strongly polar solvents, e.g. amines such as N-methylpyrrolidone and water.

Aqueous use forms can be prepared from emulsion concentrates, suspensions, pastes, wettable powders or water-dispersible granules by adding water. To prepare emulsions, pastes or oil dispersions, the substrates substances, as such or dissolved in an oil or solvent, can be homogenized in water by means of wetting agent, tackifier, dispersant or emulsifier. However, it is also possible to prepare concentrates composed of active substance, wetting agent, tackifier, dispersant or emulsifier and, if appropriate, solvent or oil, and these concentrates are suitable for dilution with water.

Suitable surfactants (adjuvants) are the alkali metal, alkaline earth metal and ammonium salts of aromatic sulfonic acids, e.g. ligno-, phenol-, naphthalene- and dibutylnaphthalenesulfonic acid, and of fatty acids, of alkyl- and alkylaryl sulfonates, of alkyl sulfates, lauryl ether sulfates and fatty alcohol sulfates, and salts of sulfated hexa-, hepta- and octadecanols, and of fatty alcohol glycol ether, condensates of sulfonated naphthalene and its derivatives with formaldehyde, condensates of naphthalene, or of the naphthalenesulfonic acids, with phenol and formaldehyde, polyoxyethylene octylphenyl ether, ethoxylated isooctyl-, octyl- or nonylphenol, alkylphenyl and tributylphenyl polyglycol ether, alkylaryl polyether alcohols, isotridecyl alcohol, fatty alcohol/ethylene oxide condensates, ethoxylated castor oil, polyoxyethylene alkyl ethers or polyoxypropylene alkyl ethers, lauryl alcohol polyglycol ether acetate, sorbitol esters, lignin-sulfite waste liquors or methylcellulose.

Powders, materials for spreading and dusts can be prepared by mixing or concomitantly grinding the active substances with a solid carrier.

Granules, e.g. coated granules, impregnated granules and homogeneous granules, can be prepared by binding the active ingredients to solid carriers. Solid carriers are mineral earths such as silicas, silica gels, silicates, talc, kaolin, limestone, lime, chalk, bole, loess, clay, dolomite, diatomaceous earth, calcium sulfate, magnesium sulfate, magnesium oxide, ground synthetic materials, fertilizers such as ammonium sulfate, ammonium phosphate, ammonium nitrate, ureas and products of vegetable origin such as cereal meal, tree bark meal, wood meal and nutshell meal, cellulose powders and other solid carriers.

The concentrations of the compounds of the formula I in the ready-to-use products can be varied within wide ranges. In general, the formulations comprise from 0.001 to 98% by weight, preferably 0.01 to 95% by weight, of at least one active ingredient. The active ingredients are employed in a purity of from 90% to 100%, preferably 95% to 100% (according to NMR spectrum).

The compounds I according to the invention can be formulated, for example, as follows:

I. 20 parts by weight of the compound No. 2.01 are dissolved in a mixture composed of 80 parts by weight of alkylated benzene, 10 parts by weight of the adduct of 8 to 10 mol of ethylene oxide and 1 mol of oleic acid N-monoethanolamide, parts by weight of calcium dodecylbenzenesulfonate and 5 parts by weight of the adduct of 40 mol of ethylene oxide and 1 mol of castor oil. Pouring the solution into 100,000 parts by weight of water and finely distributing it therein gives an aqueous dispersion which comprises 0.02% by weight of the active ingredient.

II. 20 parts by weight of the compound No. 2.03 are dissolved in a mixture composed of 40 parts by weight of cyclohexanone, 30 parts by weight of isobutanol, 20 parts by weight of the adduct of 7 mol of ethylene oxide and 1 mol of isooctylphenol and 10 parts by weight of the adduct of 40 mol of ethylene oxide and 1 mol of castor oil. Pouring the solution into 100,000 parts by weight of water and finely distributing it therein gives an aqueous dispersion which comprises 0.02% by weight of the active ingredient.

III. 20 parts by weight of the active ingredient No. 2.05 are dissolved in a mixture composed of 25 parts by weight of cyclohexanone, 65 parts by weight of a mineral oil fraction of boiling point 210 to 280° C. and 10 parts by weight of the adduct of 40 mol of ethylene oxide and 1 mol of castor oil. Pouring the solution into 100,000 parts by weight of water and finely distributing it therein gives an aqueous dispersion which comprises 0.02% by weight of the active ingredient.

IV. 20 parts by weight of the active ingredient No. 2.06 are mixed thoroughly with 3 parts by weight of sodium diisobutylnaphthalenesulfonate, 17 parts by weight of the sodium salt of a lignosulfonic acid from a sulfite waste liquor and 60 parts by weight of pulverulent silica gel and the mixture is ground in a hammer mill. Finely distributing the mixture in 20,000 parts by weight of water gives a spray mixture which comprises 0.1% by weight of the active ingredient.

V. 3 parts by weight of the active ingredient No. 2.09 are mixed with 97 parts by weight of finely divided kaolin. This gives a dust which comprises 3% by weight of the active ingredient.

VI. 20 parts by weight of the active ingredient No. 2.11 are mixed intimately with 2 parts by weight of calcium dodecylbenzenesulfonate, 8 parts by weight of fatty alcohol polyglycol ether, 2 parts by weight of the sodium salt of a phenol/urea/formaldehyde condensate and 68 parts by weight of a paraffinic mineral oil. This gives a stable oily dispersion.

VII. 1 part by weight of the compound 2.12 is dissolved in a mixture composed of 70 parts by weight of cyclohexanone, 20 parts by weight of ethoxylated isooctylphenol and 10 parts by weight of ethoxylated castor oil. This gives a stable emulsion concentrate.

VIII. 1 part by weight of the compound 2.07 is dissolved in a mixture composed of 80 parts by weight of cyclohexanone and 20 parts by weight of Wettol® EM 31 (non-ionic emulsifier based on ethoxylated castor oil). This gives a stable emulsion concentrate.

The active ingredients of the formula I, or the herbicidal compositions, can be applied pre- or post-emergence. If the active ingredients are less well tolerated by certain crop plants, application techniques may be used in which the herbicidal compositions are sprayed, with the aid of the spray apparatus, in such a way that they come into as little contact, if any, with the leaves of the sensitive crop plants while the active ingredients reach the leaves of undesirable plants which grow underneath, or the bare soil (post-directed, lay-by).

To widen the spectrum of action and to achieve synergistic effects, the compounds of the formula I can be mixed and applied jointly with a large number of representatives of other groups of herbicidally or growth-regulatory active ingredients. Suitable components in mixtures are, for example, 1,2,4-thiadiazoles, 1,3,4-thiadiazoles, amides, aminophosphoric acid and its derivatives, aminotriazoles, anilides, (het)aryloxyalkanoic acids and their derivatives, benzoic acid and its derivatives, benzothiadiazinones, 2-aroyl-1,3-cyclohexanediones, hetaryl aryl ketones, benzylisoxazolidinones, meta-CF₃-phenyl derivatives, carbamates, quinolinecarboxylic acid and its derivatives, chloroacetanilides, cyclohexenone oxime ethers, diazines, dichloropropionic acid and its derivatives, dihydrobenzofurans, dihydrofuran-3-ones, dinitroanilines, dinitrophenols, diphenyl ethers, dipyridyls, halocarboxylic acids and their derivatives, ureas, 3-phenyluracils, imidazoles, imidazolinones, N-phenyl-3,4,5,6-tetrahydrophthalimides, oxadiazoles, oxiranes, phenols, aryloxy- and hetaryloxyphenoxypropionic esters, phenylacetic acid and its derivatives, 2-phenylpropionic acid and its derivatives, pyrazoles, phenylpyrazoles, pyridazines, pyridinecarboxylic acid and its derivatives, pyrimidyl ethers, sulfonamides, sulfonylureas, triazines, triazinones, triazolinones, triazolecarboxamides and uracils.

Moreover, it may be advantageous to also apply the compounds of the formula I, alone or in combination with other herbicides, in the form of a mixture with other crop protection agents, for example with pesticides or agents for controlling phytopathogenic fungi or bacteria. Also of interest is the miscibility with mineral salt solutions which are employed for treating nutritional and trace element deficiencies. Non-phytotoxic oils and oil concentrates can also be added.

The rates of application of active ingredient are from 0.001 to is 3.0, preferably 0.01 to 1.0, kg/ha active substance (a.s.), depending on the purpose of the control measures, the season, the target plants and the growth stage.

USE EXAMPLES

The herbicidal action of the 2-benzoylcyclohexane-1,3-diones of the formula I was demonstrated by the following greenhouse experiments:

The culture containers used were plastic pots containing loamy sand with approximately 3.0% of humus as substrate. The seeds of the test plants were sown separately for each species.

For the pre-emergence treatment, the active ingredients, suspended or emulsified in water, were applied directly after sowing by means of finely distributing nozzles. The containers were irrigated gently to promote germination and growth and subsequently covered with translucent plastic hoods until the plants had rooted. This cover caused uniform germination of the test plants unless this was adversely affected by the active ingredients.

For the post-emergence treatment, the test plants were first grown to a plant height of from 3 to 15 cm, depending on the plant habit, and then treated with the active ingredients which had been suspended or emulsified in water. To this end, the test plants were either sown directly and grown in the same containers, or they were first grown separately as seedlings and transplanted into the test containers a few days prior to treatment. The rate of application for the post-emergence treatment was 0.125 or 0.0625 kg/ha a.s. Depending on the species, the plants were kept at from 10-25° C. and 20-35° C., respectively. The test period extended over 2 to 4 weeks. During this time, the plants were tended, and their response to the individual treatments was evaluated.

Evaluation was carried out using a scale of from 0 to 100. 100 means no emergence of the plants, or complete destruction of at least the aerial parts, and 0 means no damage or normal course of growth.

The plants used in the greenhouse experiments belonged to the following species:

Scientific name Common name Chenopodium album lambsquarters (goosefoot) Ipomoea spp. morning glory Polygenum persicaria ladysthumb Solanum nigrum black nightshade Zea mays Indian corn

The compound 2.01 (Table 2), when applied post-emergence at rates of 0.125 and 0.0625 kg/ha (a.s.), had a very good effect against the abovementioned mono- and dicotyledonous harmful plants combined with good tolerance in Indian corn. 

We claim:
 1. A 2-benzoylcyclohexane-1,3-dione of formula I

where the variables have the following meanings: R¹, R² are hydrogen, nitro, halogen, cyano, thiocyanato, C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₁-C₆-alkoxy-C₁-C₆-alkyl, C₂-C₆-alkenyl, C₂-C₆-alkynyl, —OR⁵, —OCOR⁶, —OSO₂R⁶, —SH, —S(O)_(n)R⁷, —SO₂OR⁵, —SO₂NR⁵R⁸, —NR⁸SO₂R⁶ or —NR⁸COR⁶; R³ is hydrogen, C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₃-C₆-alkenyl or C₃-C₆-alkynyl; R⁴ is hydrogen, C₁-C₆-alkyl, C₃-C₆-cycloalkyl, C₃-C₆-alkenyl, C₄-C₆-cycloalkenyl, C₃-C₆-alkynyl, —COR⁹, —CO₂R⁹, —COSR⁹ or —CONR⁸R⁹, it being possible for the abovementioned alkyl, cycloalkyl, alkenyl, cycloalkenyl and alkynyl radicals and for R⁹ of the radicals —COR⁹, —CO₂R⁹, —COSR⁹ and —CONR⁸R⁹ to be partially or fully halogenated and/or to have attached to them one to three of the following groups: hydroxyl, mercapto, amino, cyano, R¹⁰, —OR¹⁰, —SR¹⁰, —NR⁸R¹⁰, ═NOR¹⁰, —OCOR¹⁰, —SCOR¹⁰, —NR⁸COR¹⁰, —CO₂R¹⁰, —COSR¹⁰, —CONR⁸R¹⁰, C₁-C₄-alkyliminooxy, C₁-C₄-alkoxyamino, C₁-C₄-alkylcarbonyl, C₁-C₄-alkoxy-C₂-C₆-alkoxycarbonyl, C₁-C₄-alkylsulfonyl, heterocyclyl, heterocyclyloxy, phenyl, phenyl-C₁-C₄-alkyl, hetaryl, phenoxy, phenyl-C₁-C₄-alkoxy and hetaryloxy, it being possible for the eight last-mentioned radicals, in turn, to be substituted; X is oxygen or sulfur; z is oxygen or NR⁸; m is 0 or 1; n is 0, 1 or 2; R⁵ is hydrogen, C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₁-C₆-alkoxy-C₂-C₆-alkyl, C₃-C₆-alkenyl or C₃-C₆-alkynyl; R⁶ is C₁-C₆-alkyl or C₁-C₆-haloalkyl; R⁷ is C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₁-C₆-alkoxy-C₂-C₆-alkyl, C₃-C₆-alkenyl or C₃-C₆-alkynyl; R⁸ is hydrogen or C₁-C₆-alkyl; R⁹ is C₁-C₆-alkyl, C₃-C₆-alkenyl, C₃-C₆-alkynyl, phenyl or benzyl; R¹⁰ is C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₃-C₆-alkenyl or C₃-C₆-alkynyl; Q is a cyclohexane-1,3-dione ring of formula II

wherein R¹¹, R¹², R¹⁴ and R¹⁶ are hydrogen or C₁-C₄-alkyl; R¹³ is hydrogen, C₁-C₄-alkyl or C₃-C₄-cycloalkyl, it being possible for the two last-mentioned groups to have attached to them one to three of the following substituents: halogen, C₁-C₄-alkylthio or C₁-C₄-alkoxy; or is tetrahydropyran-2-yl, tetrahydropyran-3-yl, tetrahy-dropyran-4-yl, tetrahydrothiopyran-2-yl, tetrahydrothio-pyran-3-yl, tetrahydrothiopyran-4-yl, 1,3-dioxolan-2-yl, 1,3-dioxan-2-yl, 1,4-dioxan-2-yl, 1,3-oxathiolan-2-yl, 1,3-oxathian-2-yl, 1,3-dithiolan-2-yl or 1,3-di-thian-2-yl, it being possible for the 6 last-mentioned radicals to be substituted by one to three C₁-C₄-alkyl radicals; R¹⁵ is hydrogen, C₁-C₄-alkyl or C₁-C₆-alkoxycarbonyl; or R¹³ and R¹⁶ together form a π bond or a three to six-membered carbocyclic ring; or the CR¹³R¹⁴ unit represents a C═O group; where m is 1 if R³ is hydrogen; or an agriculturally useful salt thereof.
 2. The 2-benzoylcyclohexane-1,3-dione of formula I defined in claim 1 wherein R¹ is nitro, halogen, cyano, thiocyanato, C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₁-C₆-alkoxy-C₁-C₆-alkyl, C₂-C₆-alkenyl, C₂-C₆-alkynyl, —OR⁵ or —S(O)_(n)R⁷; R² is hydrogen or a radical as mentioned above for R¹.
 3. The 2-benzoylcyclohexane-1,3-dione of formula I defined in claim 1 wherein m is
 1. 4. The 2-benzoylcyclohexane-1,3-dione defined in claim 1 which is of formula Ia


5. A process for the preparation of the 2-benzoylcyclo-hexane-1,3-dione of formula I defined in claim 1, which comprises acylating an unsubstituted or substituted cyclohexane-1,3-dione Q with an activated carboxylic acid IIIα or with a carboxylic acid IIIβ,

where L¹ is a nucleophilically displaceable leaving group, and, if appropriate, subjecting the acylation product to a rearrangement reaction in the presence of a catalyst to give the compounds I.
 6. A benzoic acid derivative of formula IIIa

where R¹, R² are nitro, halogen, cyano, thiocyanato, C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₁-C₆-alkoxy-C₁-C₆-alkyl, C₂-C₆-alkenyl, C₂-C₆-alkynyl, —OR⁵ or —S(O)_(n)R⁷; R³ is hydrogen, C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₃-C₆-alkenyl or C₃-C₆-alkynyl; R⁴ is hydrogen, C₁-C₆-alkyl, C₃-C₆-cycloalkyl, C₃-C₆-alkenyl, C₄-C₆-cycloalkenyl, C₃-C₆-alkynyl, —COR⁹, —CO₂R⁹, —COSR⁹ or —CONR⁸R⁹, it being possible for the abovementioned alkyl, cycloalkyl, alkenyl, cycloalkenyl and alkynyl radicals and for R⁹ of the radicals —COR⁹, —CO₂R⁹, —COSR⁹ and —CONR⁸R⁹ to be partially or fully halogenated and/or to have attached to them one to three of the following groups: hydroxyl, mercapto, amino, cyano, R¹⁰, —OR¹⁰, —SR¹⁰, —NR⁸R¹⁰, ═NOR¹⁰, —OCOR¹⁰, —SCOR¹⁰, —NR⁸COR¹⁰, —CO₂R¹⁰, —COSR¹⁰, —CONR⁸R¹⁰, C₁-C₄-alkyliminooxy, C₁-C₄-alkoxyamino, C₁-C₄-alkylcarbonyl, C₁-C₄-alkoxy-C₂-C₆-alkoxycarbonyl, C₁-C₄-alkylsulfonyl, heterocyclyl, heterocyclyloxy, phenyl, phenyl-C₁-C₄-alkyl, hetaryl, phenoxy, phenyl-C₁-C₄-alkoxy and hetaryloxy, it being possible for the eight last-mentioned radicals, in turn, to be substituted; X is oxygen or sulfur; Z is oxygen or NR⁸; m is 1; n is 0, 1 or 2; R⁵ is hydrogen, C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₁-C₆-alkoxy-C₂-C₆-alkyl, C₃-C₆-alkenyl or C₃-C₆-alkynyl; R 7 is C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₁-C₆-alkoxy-C₂-C₆-alkyl, C₃-C₆-alkenyl or C₃-C₆-alkynyl; R¹⁷ is hydroxyl or a radical which can be removed by hydrolysis; where R⁴ is not hydrogen if Z is NH and R¹ and R² are chlorine.
 7. The benzoic acid derivative of formula IIIa defined in claim 6, wherein R¹⁷ is halogen, hydroxyl or C₁-C₆-alkoxy.
 8. A composition comprising a herbicidally active amount of at least one 2-benzoylcyclohexane-1,3-dione of formula I or of an agriculturally useful salt of I defined in claim 1 and auxiliaries conventionally used for the formulation of crop protection products.
 9. A process for the preparation of herbicidally active composition defined in claim 8, which comprises mixing a herbicidally active amount of at least one 2-benzoyl-cyclohexane-1,3-dione of formula I or of an agriculturally useful salt of I and auxiliaries conventionally used for the formulation of crop protection products.
 10. A method of controlling undesirable vegetation, which comprises allowing a herbicidally active amount of at least one 2-benzoylcyclohexane-1,3-dione of formula I or of an agriculturally useful salt of I defined in claim 1 to act on plants, their environment and/or on seeds.
 11. The 2-benzoylcyclohexane-1,3-dione of formula I defined in claim 1 wherein R³ is hydrogen, methyl, ethyl, propyl, butyl, difluoromethyl or trifluoromethyl.
 12. The 2-benzoylcyclohexane-1,3-dione of formula I defined in claim 1 wherein X is oxygen.
 13. The 2-benzoylcyclohexane-1,3-dione of formula I defined in claim 1 wherein Z is oxygen, NH or N—CH₃.
 14. The 2-benzoylcyclohexane-1,3-dione of formula I defined in claim 1 wherein R¹¹, R¹², R¹⁴ and R¹⁵ are each hydrogen, methyl or ethyl.
 15. The 2-benzoylcyclohexane-1,3-dione of formula I defined in claim 1 wherein R¹⁵ is hydrogen, methyl or ethyl.
 16. The 2-benzoylcyclohexane-1,3-dione of formula I defined in claim 1 wherein CR¹³R¹⁴ represents a C═O group.
 17. The 2-benzoylcyclohexane-1,3-dione defined in claim 1 which is of formula Ia′

wherein R¹ is halogen or C₁-C₄-alkylsulfonyl; R² is halogen or C₁-C₄-alkyl; R³ is hydrogen or C₁-C₄-alkyl; R⁴ is hydrogen, C₁-C₆-alkyl, C₃-C₆-alkenyl, it being possible for the two last-mentioned substituents to be partially or fully halogenated and/or to have attached to them one to three of the following froups: phenyl, phenyl-C₁-C₄-alkyl, hetaryl or phenoxy, it being possible for the 4 last-mentioned radicals to be partially or fully halogenated; X is oxygen; Z is oxygen or NH; m is 0 or 1; R¹¹, R¹², R¹⁴, R¹⁵ and R¹⁶ are hydrogen or C₁-C₄-alkyl; R¹³ is hydrogen, C₁-C₄-alkyl, tetrahydropyran-3-yl, tetrahydro-thiopyran-3-yl or 1,4-dioxan-2-yl; or the CR¹³R¹⁴ unit represents a C═O group.
 18. The 2-benzoylcyclohexane-1,3-dione of formula I defined in claim 1 wherein R¹⁵ is H or C₁-C₄-alkyl.
 19. The 2-benzoylcyclohexane-1,3-dione of formula I defined in claim 4 wherein R¹⁵ is H or C₁-C₄-alkyl. 